Details for New Drug Application (NDA): 071972
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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 071972
Tradename: | PROPRANOLOL HYDROCHLORIDE |
Applicant: | Impax Labs Inc |
Ingredient: | propranolol hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 071972
Mechanism of Action | Adrenergic beta-Antagonists |
Medical Subject Heading (MeSH) Categories for 071972
Suppliers and Packaging for NDA: 071972
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | TABLET;ORAL | 071972 | ANDA | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8413 | 0615-8413-39 | 30 TABLET in 1 BLISTER PACK (0615-8413-39) |
PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | TABLET;ORAL | 071972 | ANDA | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8417 | 0615-8417-39 | 30 TABLET in 1 BLISTER PACK (0615-8417-39) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Apr 6, 1988 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
Approval Date: | Apr 6, 1988 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 40MG | ||||
Approval Date: | Apr 6, 1988 | TE: | AB | RLD: | No |
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