Details for New Drug Application (NDA): 078341
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The generic ingredient in FINASTERIDE is finasteride; tadalafil. There are fourteen drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the finasteride; tadalafil profile page.
Summary for 078341
Tradename: | FINASTERIDE |
Applicant: | Aurobindo Pharma |
Ingredient: | finasteride |
Patents: | 0 |
Pharmacology for NDA: 078341
Mechanism of Action | 5-alpha Reductase Inhibitors |
Medical Subject Heading (MeSH) Categories for 078341
Suppliers and Packaging for NDA: 078341
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
FINASTERIDE | finasteride | TABLET;ORAL | 078341 | ANDA | A-S Medication Solutions | 50090-6940 | 50090-6940-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-6940-0) |
FINASTERIDE | finasteride | TABLET;ORAL | 078341 | ANDA | A-S Medication Solutions | 50090-6940 | 50090-6940-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6940-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Oct 30, 2007 | TE: | AB | RLD: | No |
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