Details for New Drug Application (NDA): 072575
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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 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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