Details for New Drug Application (NDA): 070176
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The generic ingredient in PROPRANOLOL HYDROCHLORIDE is hydrochlorothiazide; propranolol hydrochloride. There are thirty-two drug master file entries for this compound. Additional details are available on the hydrochlorothiazide; propranolol hydrochloride profile page.
Summary for 070176
Tradename: | PROPRANOLOL HYDROCHLORIDE |
Applicant: | Watson Labs |
Ingredient: | propranolol hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 070176
Mechanism of Action | Adrenergic beta-Antagonists |
Medical Subject Heading (MeSH) Categories for 070176
Suppliers and Packaging for NDA: 070176
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | TABLET;ORAL | 070176 | ANDA | Amneal Pharmaceuticals of New York LLC | 0115-1660 | 0115-1660-01 | 100 TABLET in 1 BOTTLE, PLASTIC (0115-1660-01) |
PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | TABLET;ORAL | 070176 | ANDA | Amneal Pharmaceuticals of New York LLC | 0115-1660 | 0115-1660-03 | 1000 TABLET in 1 BOTTLE, PLASTIC (0115-1660-03) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
Approval Date: | May 13, 1986 | TE: | AB | RLD: | No |
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