Details for New Drug Application (NDA): 070177
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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 070177
| Tradename: | PROPRANOLOL HYDROCHLORIDE |
| Applicant: | Watson Labs |
| Ingredient: | propranolol hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 070177
| Mechanism of Action | Adrenergic beta-Antagonists |
Medical Subject Heading (MeSH) Categories for 070177
Suppliers and Packaging for NDA: 070177
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | TABLET;ORAL | 070177 | ANDA | NuCare Pharmaceuticals,Inc. | 68071-3576 | 68071-3576-1 | 120 TABLET in 1 BOTTLE, PLASTIC (68071-3576-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 40MG | ||||
| Approval Date: | May 13, 1986 | TE: | AB | RLD: | No | ||||
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