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NORTHEAST Pharmaceutical Group Shenyang NO.1 Pharmaceutical Co., Ltd.
  • Founded in:

    1989-01-25
  • Country:

    China China
  • Address:

    No. 8 Kunming Lake Street, Shenyang Economic and Technological Development Zone
  • Tax NO.:

    91210106242656694M
  • Registered Funds:

    80 million yuan
  • Website:

  • Email:

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Compound aluminum hydroxide tablets
This product is a compound preparation. Each tablet contains the main ingredients of aluminum hydroxide 0.245 grams, magnesium trisilicate 0.105 grams, and belladonna fluid extract 0.0026 milliliters.
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Aluminum hydroxide

Can neutralize excess stomach acid

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Can neutralize excess stomach acid

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Magnesium trisilicate

Can neutralize excess stomach acid

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Extract Belladonna soft liquid and powder

It can not only inhibit gastric juice secretion, relieve gastric smooth muscle spasm, but also delay gastric emptying.

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It can not only inhibit gastric juice secretion, relieve gastric smooth muscle spasm, but also delay gastric emptying.

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Mint Lozenges
Each tablet contains the following active ingredients: 2 mg menthol, 5 mg sodium benzoate, and 0.6 mg chlorobutanol.
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DL-Menthol

It is a local irritant that can selectively act on the cold receptors of the mucosa, produce a cold reflex, cause the mucosal blood vessels to contract, and produce a therapeutic effect. It has a cooling effect on the mucosa; it can cause blood vessels to contract and reduce edema when used on inflamed mucosa.

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It is a local irritant that can selectively act on the cold receptors of the mucosa, produce a cold reflex, cause the mucosal blood vessels to contract, and produce a therapeutic effect. It has a cooling effect on the mucosa; it can cause blood vessels to contract and reduce edema when used on inflamed mucosa.

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Sodium benzoate

The active ingredient of this product, menthol, is a local irritant. When used locally, it can selectively act on the cold receptors of the mucosa, produce a cold reflex, cause the mucosal blood vessels to contract, and produce a therapeutic effect. When used on the mucosa, it has a cooling effect; when used on inflamed mucosa, it can cause blood vessels to contract and reduce edema.

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The active ingredient of this product, menthol, is a local irritant. When used locally, it can selectively act on the cold receptors of the mucosa, produce a cold reflex, cause the mucosal blood vessels to contract, and produce a therapeutic effect. When used on the mucosa, it has a cooling effect; when used on inflamed mucosa, it can cause blood vessels to contract and reduce edema.

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Chlorobutanol

The active ingredient of this product, menthol, is a local irritant. When used locally, it can selectively act on the cold receptors of the mucosa, produce a cold reflex, cause the mucosal blood vessels to contract, and produce a therapeutic effect. When used on the mucosa, it has a cooling effect; when used on inflamed mucosa, it can cause blood vessels to contract and reduce edema.

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The active ingredient of this product, menthol, is a local irritant. When used locally, it can selectively act on the cold receptors of the mucosa, produce a cold reflex, cause the mucosal blood vessels to contract, and produce a therapeutic effect. When used on the mucosa, it has a cooling effect; when used on inflamed mucosa, it can cause blood vessels to contract and reduce edema.

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Propranolol Hydrochloride Tablets
The main ingredient of this product and its chemical name are: 1-isopropylamino-3-(1-naphthyloxy)-2-propanol hydrochloride.
Name Description Content CAS NO. Registered Holders
Propanolol

1. It is a non-selective competitive inhibitor of adrenergic β-receptor blocker, blocking β1 and β2 receptors on the heart, reducing the contractile force and contractile speed of the heart, while inhibiting the contraction of vascular smooth muscle, reducing myocardial oxygen consumption, and is used to treat angina pectoris; 2. It inhibits the adrenergic excitement of cardiac pacemaker potentials and is used to treat arrhythmias; 3. It can inhibit the release of renin and reduce cardiac output through central and adrenergic neuron blocking, and is used to treat hypertension; 4. It competitively antagonizes the effects of isoproterenol and norepinephrine, blocks β2 receptors, reduces plasma renin activity, and has a significant anti-platelet aggregation effect.

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1. It is a non-selective competitive inhibitor of adrenergic β-receptor blocker, blocking β1 and β2 receptors on the heart, reducing the contractile force and contractile speed of the heart, while inhibiting the contraction of vascular smooth muscle, reducing myocardial oxygen consumption, and is used to treat angina pectoris; 2. It inhibits the adrenergic excitement of cardiac pacemaker potentials and is used to treat arrhythmias; 3. It can inhibit the release of renin and reduce cardiac output through central and adrenergic neuron blocking, and is used to treat hypertension; 4. It competitively antagonizes the effects of isoproterenol and norepinephrine, blocks β2 receptors, reduces plasma renin activity, and has a significant anti-platelet aggregation effect.

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Adenosine triphosphate disodium for injection
Chemical name: adenosine-5-triphosphate disodium salt, molecular formula: C10H14N5Na2O13P3 molecular weight: 551.15
Name Description Content CAS NO. Registered Holders
Adenosine5'-(tetrahydrogen triphosphate), disodiuM salt, trihydrate (9CI)

It is a coenzyme that improves the body's metabolism and participates in the metabolism of fat, protein, sugar, nucleic acid and nucleotides in the body. It is also the main source of energy in the body. When energy is needed for absorption, secretion, muscle contraction and biochemical synthesis reactions, adenosine triphosphate is decomposed into adenosine diphosphate and phosphate groups, and energy is released at the same time. Animal experiments can inhibit the slow calcium ion influx of slow-reacting fibers, block or delay the forward conduction in the atrioventricular node reentry pathway, and large doses may also block or delay the forward and reverse conduction of the bypass pathway; in addition, it also has a short-term and strong effect of enhancing the vagus nerve, thereby terminating arrhythmias caused by atrioventricular node reentry and bypass reentry mechanisms.

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It is a coenzyme that improves the body's metabolism and participates in the metabolism of fat, protein, sugar, nucleic acid and nucleotides in the body. It is also the main source of energy in the body. When energy is needed for absorption, secretion, muscle contraction and biochemical synthesis reactions, adenosine triphosphate is decomposed into adenosine diphosphate and phosphate groups, and energy is released at the same time. Animal experiments can inhibit the slow calcium ion influx of slow-reacting fibers, block or delay the forward conduction in the atrioventricular node reentry pathway, and large doses may also block or delay the forward and reverse conduction of the bypass pathway; in addition, it also has a short-term and strong effect of enhancing the vagus nerve, thereby terminating arrhythmias caused by atrioventricular node reentry and bypass reentry mechanisms.

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Adenosine triphosphate disodium for injection
Chemical name: adenosine-5-triphosphate disodium salt, molecular formula: C10H14N5Na2O13P3 molecular weight: 551.15
Name Description Content CAS NO. Registered Holders
Adenosine5'-(tetrahydrogen triphosphate), disodiuM salt, trihydrate (9CI)

It is a coenzyme that improves the body's metabolism and participates in the metabolism of fat, protein, sugar, nucleic acid and nucleotides in the body. It is also the main source of energy in the body. When energy is needed for absorption, secretion, muscle contraction and biochemical synthesis reactions, adenosine triphosphate is decomposed into adenosine diphosphate and phosphate groups, and energy is released at the same time. Animal experiments can inhibit the slow calcium ion influx of slow-reacting fibers, block or delay the forward conduction in the atrioventricular node reentry pathway, and large doses may also block or delay the forward and reverse conduction of the bypass pathway; in addition, it also has a short-term and strong effect of enhancing the vagus nerve, thereby terminating arrhythmias caused by atrioventricular node reentry and bypass reentry mechanisms.

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It is a coenzyme that improves the body's metabolism and participates in the metabolism of fat, protein, sugar, nucleic acid and nucleotides in the body. It is also the main source of energy in the body. When energy is needed for absorption, secretion, muscle contraction and biochemical synthesis reactions, adenosine triphosphate is decomposed into adenosine diphosphate and phosphate groups, and energy is released at the same time. Animal experiments can inhibit the slow calcium ion influx of slow-reacting fibers, block or delay the forward conduction in the atrioventricular node reentry pathway, and large doses may also block or delay the forward and reverse conduction of the bypass pathway; in addition, it also has a short-term and strong effect of enhancing the vagus nerve, thereby terminating arrhythmias caused by atrioventricular node reentry and bypass reentry mechanisms.

51963-61-2 0
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