Details for New Drug Application (NDA): 212329
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The generic ingredient in DOXAZOSIN MESYLATE is doxazosin mesylate. There are fourteen drug master file entries for this compound. Thirty-two suppliers are listed for this compound. Additional details are available on the doxazosin mesylate profile page.
Summary for 212329
Tradename: | DOXAZOSIN MESYLATE |
Applicant: | Unichem |
Ingredient: | doxazosin mesylate |
Patents: | 0 |
Pharmacology for NDA: 212329
Mechanism of Action | Adrenergic alpha-Antagonists |
Medical Subject Heading (MeSH) Categories for 212329
Suppliers and Packaging for NDA: 212329
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DOXAZOSIN MESYLATE | doxazosin mesylate | TABLET;ORAL | 212329 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-351 | 29300-351-01 | 100 TABLET in 1 BOTTLE (29300-351-01) |
DOXAZOSIN MESYLATE | doxazosin mesylate | TABLET;ORAL | 212329 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-351 | 29300-351-10 | 1000 TABLET in 1 BOTTLE (29300-351-10) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 1MG BASE | ||||
Approval Date: | Jan 10, 2024 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 2MG BASE | ||||
Approval Date: | Jan 10, 2024 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 4MG BASE | ||||
Approval Date: | Jan 10, 2024 | TE: | AB | RLD: | No |
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