Sichuan Taihua TANG Pharmacy Co., Ltd. | Pharmaceutical Manufacturer Profile & Drug Portfolio

Sophie Cough Syrup

Stemona fluid extract, licorice fluid extract, menthol, mulberry bark fluid extract, ammonium chloride, platycodon fluid extract, ephedrine hydrochloride.

Name	CAS NO.	Registered Holders
STEMONAJAPONICA		0
Licorice extract	68916-91-6	0
DL-Menthol	89-78-1	8
Morus alba fluid extract		0
Ammonium chloride	12125-02-9	17
Platycodon extract		0
Ephedrine hydrochloride		0

Bushen Yiqi Capsule

Original silkworm moth, wolfberry, dodder seed, Cistanche deserticola, Cnidium monnieri, Epimedium, Rehmannia root, processed Polygonum multiflorum, Schisandra chinensis, Ophiopogon japonicus, Astragalus membranaceus.

Name	CAS NO.	Registered Holders
Bombyx mori		0
lycii Fructus		0
Cuscutae Semen		0
CISTANCHES HERBA		0
Cnidii Fructus		0
Epimedium P.E Icariin 10%,20% HPLC		0
REHMANNIAE RADIX PRAEPARATA		0
POLYGONI MULTIFLORI RADIX PRAEPARATA		0
Anise oil	8007-70-3	10
Ophiopogonis Radix		0
Astragali Radix		0

Bushen Yiqi Capsule

Original silkworm moth, wolfberry, dodder seed, Cistanche deserticola, Cnidium monnieri, Epimedium, Rehmannia root, processed Polygonum multiflorum, Schisandra chinensis, Ophiopogon japonicus, Astragalus membranaceus.

Name	CAS NO.	Registered Holders
Bombyx mori		0
lycii Fructus		0
Cuscutae Semen		0
CISTANCHES HERBA		0
Cnidii Fructus		0
Epimedium P.E Icariin 10%,20% HPLC		0
REHMANNIAE RADIX PRAEPARATA		0
POLYGONI MULTIFLORI RADIX PRAEPARATA		0
Anise oil	8007-70-3	10
Ophiopogonis Radix		0
Astragali Radix		0

Zidan Huoxue Capsules

Notoginseng total saponins, Salvia miltiorrhiza.

Name	Description	Content	CAS NO.	Registered Holders
Panax notoginsenosides				0
A Purple Tan				0

Heat-clearing and detoxifying oral liquid

Gypsum, honeysuckle, Scrophularia, Rehmannia root, Forsythia suspensa, Gardenia jasminoides, Scutellaria baicalensis, Gentiana scabra, Radix Isatidis, Rhizoma Anemarrhenae, Radix Ophiopogonis. Sucrose is an auxiliary ingredient.

Name	Description	CAS NO.	Registered Holders
Calcium sulfate dihydrate	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.	10101-41-4	0
LONICERAE JAPONICAE FLOS	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
Scrophulariae Radix	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
REHMANNIAE RADIX PRAEPARATA	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
Forsythiae Fructus	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
Gardeniae Fructus	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
sweet diced	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
RADIX SCUTELLARIAE	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
Borneol	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.	507-70-0	1
Isatidis Radix	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
ANEMARRHENAE RHIZOMA	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
Ophiopogonis Radix	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.		0
Sucrose	Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically. More Toxicity test: Acute toxicity test: 20 mice, half male and half female, were orally administered 150g (raw drug)/kg at a time and observed for 72 hours. No one died, and there was no abnormality in behavior and appearance. Subacute toxicity test: Rats were orally administered 60 and 90g (raw drug)/kg for 25 consecutive days. Results: There were no abnormal changes in the weight, blood picture, and electrocardiogram of each group of animals, and no pathological changes were found in the heart, liver, and kidney. The above tests show that the drug is non-toxic, safe for oral administration, and can be used clinically.	57-50-1	72