Details for New Drug Application (NDA): 071745
✉ Email this page to a colleague
NDA 071745 describes PRAZOSIN HYDROCHLORIDE, which is a drug marketed by Alembic, Am Therap, Ani Pharms, Appco, Aurobindo Pharma Ltd, Dava Pharms Inc, Granules, Lannett Co Inc, Mankind Pharma, MSN, Mylan, Novitium Pharma, Purepac Pharm, Teva Pharms, and Watson Labs, and is included in twenty-three NDAs. It is available from thirty-one suppliers. Additional details are available on the PRAZOSIN HYDROCHLORIDE profile page.
The generic ingredient in PRAZOSIN HYDROCHLORIDE is prazosin hydrochloride. There are seventeen drug master file entries for this compound. Thirty-two suppliers are listed for this compound. Additional details are available on the prazosin hydrochloride profile page.
The generic ingredient in PRAZOSIN HYDROCHLORIDE is prazosin hydrochloride. There are seventeen drug master file entries for this compound. Thirty-two suppliers are listed for this compound. Additional details are available on the prazosin hydrochloride profile page.
Summary for 071745
| Tradename: | PRAZOSIN HYDROCHLORIDE |
| Applicant: | Teva Pharms |
| Ingredient: | prazosin hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 071745
| Mechanism of Action | Adrenergic alpha-Antagonists |
Medical Subject Heading (MeSH) Categories for 071745
Suppliers and Packaging for NDA: 071745
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PRAZOSIN HYDROCHLORIDE | prazosin hydrochloride | CAPSULE;ORAL | 071745 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-4067 | 0093-4067-01 | 100 CAPSULE in 1 BOTTLE (0093-4067-01) |
| PRAZOSIN HYDROCHLORIDE | prazosin hydrochloride | CAPSULE;ORAL | 071745 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-4067 | 0093-4067-10 | 1000 CAPSULE in 1 BOTTLE (0093-4067-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 5MG BASE | ||||
| Approval Date: | Sep 12, 1988 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 1MG BASE | ||||
| Approval Date: | Sep 12, 1988 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 2MG BASE | ||||
| Approval Date: | Sep 12, 1988 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
