Suppliers and packages for NDA: 071611
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071611
Listed suppliers include manufacturers, repackagers, relabelers, and private labeling entitities.
Applicant | Tradename | Generic Name | Dosage | NDA | NDA/ANDA | Supplier | Package Code | Package | Marketing Start |
---|---|---|---|---|---|---|---|---|---|
Actavis Labs Fl Inc | CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | TABLET;ORAL | 071611 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-3420-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-3420-01) | 2021-07-20 |
Actavis Labs Fl Inc | CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | TABLET;ORAL | 071611 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-3421-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-3421-01) | 2021-07-20 |
Actavis Labs Fl Inc | CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | TABLET;ORAL | 071611 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-3422-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-3422-01) | 2021-07-20 |
Actavis Labs Fl Inc | CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | TABLET;ORAL | 071611 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-3422-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-3422-05) | 2021-07-20 |
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >NDA/ANDA | >Supplier | >Package Code | >Package | >Marketing Start |