Details for New Drug Application (NDA): 071745
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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 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 |
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