Details for New Drug Application (NDA): 070979
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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 070979
Tradename: | PROPRANOLOL HYDROCHLORIDE |
Applicant: | Hikma |
Ingredient: | propranolol hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 070979
Mechanism of Action | Adrenergic beta-Antagonists |
Medical Subject Heading (MeSH) Categories for 070979
Suppliers and Packaging for NDA: 070979
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | SOLUTION;ORAL | 070979 | ANDA | Hikma Pharmaceuticals USA Inc. | 0054-3727 | 0054-3727-63 | 500 mL in 1 BOTTLE, PLASTIC (0054-3727-63) |
PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | SOLUTION;ORAL | 070979 | ANDA | Pharmaceutical Associates, Inc. | 0121-0908 | 0121-0908-40 | 4 TRAY in 1 CASE (0121-0908-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0908-05) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 20MG/5ML | ||||
Approval Date: | May 15, 1987 | TE: | RLD: | No |
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