Details for New Drug Application (NDA): 071321
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The generic ingredient in DIAZEPAM is diazepam. There are eight drug master file entries for this compound. Forty-seven suppliers are listed for this compound. Additional details are available on the diazepam profile page.
Summary for 071321
Tradename: | DIAZEPAM |
Applicant: | Ivax Sub Teva Pharms |
Ingredient: | diazepam |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Suppliers and Packaging for NDA: 071321
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DIAZEPAM | diazepam | TABLET;ORAL | 071321 | ANDA | Teva Pharmaceuticals USA, Inc. | 0172-3926 | 0172-3926-60 | 100 TABLET in 1 BOTTLE (0172-3926-60) |
DIAZEPAM | diazepam | TABLET;ORAL | 071321 | ANDA | Teva Pharmaceuticals USA, Inc. | 0172-3926 | 0172-3926-70 | 500 TABLET in 1 BOTTLE (0172-3926-70) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Dec 10, 1986 | TE: | AB | RLD: | No |
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