Details for New Drug Application (NDA): 072575
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NDA 072575 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 twenty-nine 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 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 suppliers are listed for this compound. Additional details are available on the prazosin hydrochloride profile page.
Summary for 072575
| Tradename: | PRAZOSIN HYDROCHLORIDE |
| Applicant: | Mylan |
| Ingredient: | prazosin hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 072575
| Mechanism of Action | Adrenergic alpha-Antagonists |
Medical Subject Heading (MeSH) Categories for 072575
Suppliers and Packaging for NDA: 072575
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PRAZOSIN HYDROCHLORIDE | prazosin hydrochloride | CAPSULE;ORAL | 072575 | ANDA | Mylan Pharmaceuticals Inc. | 0378-1101 | 0378-1101-01 | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-1101-01) |
| PRAZOSIN HYDROCHLORIDE | prazosin hydrochloride | CAPSULE;ORAL | 072575 | ANDA | Mylan Pharmaceuticals Inc. | 0378-1101 | 0378-1101-10 | 1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-1101-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 5MG BASE | ||||
| Approval Date: | May 16, 1989 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 2MG BASE | ||||
| Approval Date: | May 16, 1989 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 1MG BASE | ||||
| Approval Date: | May 16, 1989 | TE: | AB | RLD: | No | ||||
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