Details for New Drug Application (NDA): 078065
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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 078065
| Tradename: | PROPRANOLOL HYDROCHLORIDE |
| Applicant: | Anda Repository |
| Ingredient: | propranolol hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 078065
| Mechanism of Action | Adrenergic beta-Antagonists |
Medical Subject Heading (MeSH) Categories for 078065
Suppliers and Packaging for NDA: 078065
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 078065 | ANDA | Nortec Development Associates, Inc | 42689-011 | 42689-011-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42689-011-01) |
| PROPRANOLOL HYDROCHLORIDE | propranolol hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 078065 | ANDA | Nortec Development Associates, Inc | 42689-011 | 42689-011-10 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42689-011-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 60MG | ||||
| Approval Date: | Jan 26, 2007 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 80MG | ||||
| Approval Date: | Jan 26, 2007 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 120MG | ||||
| Approval Date: | Jan 26, 2007 | TE: | AB | RLD: | No | ||||
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