Suppliers and packages for NDA: 078866
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078866
Listed suppliers include manufacturers, repackagers, relabelers, and private labeling entitities.
Applicant | Tradename | Generic Name | Dosage | NDA | NDA/ANDA | Supplier | Package Code | Package | Marketing Start |
---|---|---|---|---|---|---|---|---|---|
Sun Pharm | BUPROPION HYDROCHLORIDE | bupropion hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 078866 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-736-08 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-08) | 2020-03-01 |
Sun Pharm | BUPROPION HYDROCHLORIDE | bupropion hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 078866 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-736-13 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-13) | 2020-03-01 |
Sun Pharm | BUPROPION HYDROCHLORIDE | bupropion hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 078866 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-736-86 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-86) | 2020-03-01 |
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >NDA/ANDA | >Supplier | >Package Code | >Package | >Marketing Start |