Beijing Hanmi Pharmaceutical Co., Ltd. | Pharmaceutical Manufacturer Profile & Drug Portfolio

Trans-4-[(2-amino-3,5-dibromo-phenyl)methyl-amino]cyclohexanol hydrochloride

Name	Description	Content	CAS NO.	Registered Holders
Trans-4-[(2-amino-3,5-dibromo-phenyl)methyl-amino]cyclohexanol hydrochloride	This product is a mucolytic agent that can increase the secretion of serous glands in the respiratory mucosa and reduce the secretion of mucous glands, thereby reducing sputum viscosity, promoting the secretion of pulmonary surfactant, increasing bronchial ciliary movement, and making sputum easier to cough up. More This product is a mucolytic agent that can increase the secretion of serous glands in the respiratory mucosa and reduce the secretion of mucous glands, thereby reducing sputum viscosity, promoting the secretion of pulmonary surfactant, increasing bronchial ciliary movement, and making sputum easier to cough up.			0

Cetirizine Hydrochloride Oral Solution

The main ingredient of this product is cetirizine hydrochloride, and its chemical name is (±)-2-[2-[4-[(4-chlorophenyl)benzyl]-1-piperazinyl]ethoxy]acetic acid dihydrochloride.

Name	Description	Content	CAS NO.	Registered Holders
Cetirizine dihydrochloride	Selective histamine H1 receptor antagonist, no obvious anticholinergic and anti-5-hydroxytryptamine effect, not easy to pass the blood-cerebrospinal fluid barrier, clinical use of central nervous system inhibitory effect is relatively mild More Selective histamine H1 receptor antagonist, no obvious anticholinergic and anti-5-hydroxytryptamine effect, not easy to pass the blood-cerebrospinal fluid barrier, clinical use of central nervous system inhibitory effect is relatively mild		83881-52-1	54

Bacillus subtilis combined with live bacteria enteric-coated capsules

This product is a compound preparation, and its main ingredients are: Each capsule (250mg) contains: 500 million live bacteria, including 4.5108 Enterococcus faecium and 5.0107 Bacillus subtilis.

Name	Description	Content	CAS NO.	Registered Holders
Enterococcus faecium	Directly supplement normal physiological flora, inhibit pathogenic bacteria, promote digestion and absorption of nutrients, inhibit the production and absorption of enterogenic toxins, and adjust the imbalance of intestinal flora More Directly supplement normal physiological flora, inhibit pathogenic bacteria, promote digestion and absorption of nutrients, inhibit the production and absorption of enterogenic toxins, and adjust the imbalance of intestinal flora	4.5108indivual		0
EC 3.4.21.14	Directly supplement normal physiological flora, inhibit pathogenic bacteria, promote digestion and absorption of nutrients, inhibit the production and absorption of enterogenic toxins, and adjust the imbalance of intestinal flora More Directly supplement normal physiological flora, inhibit pathogenic bacteria, promote digestion and absorption of nutrients, inhibit the production and absorption of enterogenic toxins, and adjust the imbalance of intestinal flora	5.0107indivual	9014-01-1	0

Bacillus subtilis combined with live bacteria granules

This product is a compound preparation. Its main components are: every gram (1 bag) contains 37.5 mg of live bacteria freeze-dried powder, 1.35×108 Enterococcus faecium (R-026), 1.5×107 Bacillus subtilis (R-179), 10 mg of vitamin C, 0.5 mg of vitamin B1, 0.5 mg of vitamin B2, 0.5 mg of vitamin B6, 1.0 micrograms of vitamin B12, 2.0 mg of niacinamide, 20 mg of calcium lactate (equivalent to 2.6 mg of calcium), and 1.25 mg of zinc oxide (equivalent to 1.0 mg of zinc).

Name	Description	Content	CAS NO.	Registered Holders
Live bacteria freeze-dried powder	Regulate the human intestinal environment, promote the growth and reproduction of normal intestinal flora, and inhibit the growth of intestinal pathogenic bacteria More Regulate the human intestinal environment, promote the growth and reproduction of normal intestinal flora, and inhibit the growth of intestinal pathogenic bacteria	37.5mg		0
Enterococcus faecium (R-026)	Regulate the human intestinal environment, promote the growth and reproduction of normal intestinal flora, and inhibit the growth of intestinal pathogenic bacteria More Regulate the human intestinal environment, promote the growth and reproduction of normal intestinal flora, and inhibit the growth of intestinal pathogenic bacteria	1.35×10^8indivual		0
Bacillus subtilis (R-179)	Regulate the human intestinal environment, promote the growth and reproduction of normal intestinal flora, and inhibit the growth of intestinal pathogenic bacteria More Regulate the human intestinal environment, promote the growth and reproduction of normal intestinal flora, and inhibit the growth of intestinal pathogenic bacteria	1.5×10^7indivual		0
Ascorbic Acid	Necessary for infant growth and development More Necessary for infant growth and development	10mg	50-81-7	28
Thiamine chloride	Necessary for infant growth and development More Necessary for infant growth and development	0.5mg	59-43-8	9
Riboflavin	Necessary for infant growth and development More Necessary for infant growth and development	0.5mg	83-88-5	19
Vitamin B6	Necessary for infant growth and development More Necessary for infant growth and development	0.5mg	8059-24-3	13
Vitamin B12	Necessary for infant growth and development More Necessary for infant growth and development	1.0microgram	68-19-9	16
Nicotinamide	Necessary for infant growth and development More Necessary for infant growth and development	2.0mg	98-92-0	12
Calcium lactate	Provides mineral calcium to support the growth and development of infants and young children More Provides mineral calcium to support the growth and development of infants and young children	20mg	814-80-2	10
Zinc oxide	Provides trace element zinc to support the growth and development of infants and young children More Provides trace element zinc to support the growth and development of infants and young children	1.25mg	1314-13-2	21

Compound paracetamol and methyl paracetamol oral solution

This product is a compound preparation, and its components are 11.25 mg of acetaminophen, 0.6 mg of dextromethorphan hydrobromide, 93.75 μg of chlorpheniramine maleate, 0.9375 mg of methylephedrine hydrochloride, 2.5 mg of potassium guaiacol sulfonate, 33 μg of riboflavin sodium phosphate, and 1.0 mg of anhydrous caffeine per ml.

Name	Description	Content	CAS NO.	Registered Holders
Acetaminophen	After oral administration, it is rapidly and completely absorbed from the gastrointestinal tract and evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. More After oral administration, it is rapidly and completely absorbed from the gastrointestinal tract and evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid.	11.25mg	103-90-2	68
Dextromethorphan hydrobromide monohydrate	The drug takes effect half an hour after taking it, and the effect lasts for 6 hours. It is metabolized in the liver. The plasma level of dextrorphan is low, and the main metabolites are 3-methoxymorphinane, 3-hydroxy-17-methylmorphinane and 3-hydroxymorphinane. It is excreted by the kidneys, including the original and demethylated metabolites. More The drug takes effect half an hour after taking it, and the effect lasts for 6 hours. It is metabolized in the liver. The plasma level of dextrorphan is low, and the main metabolites are 3-methoxymorphinane, 3-hydroxy-17-methylmorphinane and 3-hydroxymorphinane. It is excreted by the kidneys, including the original and demethylated metabolites.	0.6mg		0
Chlorphenamine maleate	Oral absorption through the gastrointestinal tract is slow, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. More Oral absorption through the gastrointestinal tract is slow, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys.	93.75μg	113-92-8	28
L-N-METHYLEPHEDRINE HYDROCHLORIDE	After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites. More After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites.	0.9375mg		0
Potassium guaiacolsulfonate hemihydrate	After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites. More After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites.	2.5mg	78247-49-1	5
Riboflavin 5'-Monophosphate Sodium Salt	After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites. More After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites.	33μg	130-40-5	8
Caffeine	After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites. More After oral administration, the acetaminophen in this product is rapidly and completely absorbed from the gastrointestinal tract. After absorption, it is evenly distributed in body fluids. 90% to 95% is metabolized in the liver and excreted from the kidneys mainly in the form of binding with glucuronic acid. Chlorpheniramine maleate is slowly absorbed from the gastrointestinal tract after oral administration, with a bioavailability of about 25% to 50% and a protein binding rate of 72%. It takes effect 15 to 60 minutes after oral administration and is mainly metabolized by the liver. Metabolites and unmetabolized drugs are mainly excreted through the kidneys. Dextromethorphan hydrobromide takes effect half an hour after administration and lasts for 6 hours. It is metabolized in the liver. The dextrorphan content in plasma is low, mainly three metabolites: 3-methoxymorphin, 3-hydroxy-17-methylmorphin and 3-hydroxymorphin, which are excreted by the kidneys, including the original and demethylated metabolites.	1.0mg		0