Details for New Drug Application (NDA): 200739
✉ Email this page to a colleague
The generic ingredient in ALPRAZOLAM is alprazolam. There are fifteen drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the alprazolam profile page.
Summary for 200739
Tradename: | ALPRAZOLAM |
Applicant: | Natco |
Ingredient: | alprazolam |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Suppliers and Packaging for NDA: 200739
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ALPRAZOLAM | alprazolam | TABLET;ORAL | 200739 | ANDA | Proficient Rx LP | 63187-966 | 63187-966-30 | 30 TABLET in 1 BOTTLE (63187-966-30) |
ALPRAZOLAM | alprazolam | TABLET;ORAL | 200739 | ANDA | Proficient Rx LP | 63187-966 | 63187-966-60 | 60 TABLET in 1 BOTTLE (63187-966-60) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 0.25MG | ||||
Approval Date: | Apr 15, 2015 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 0.5MG | ||||
Approval Date: | Apr 15, 2015 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 1MG | ||||
Approval Date: | Apr 15, 2015 | TE: | AB | RLD: | No |
Complete Access Available with Subscription