Application 203650
- Type
- ANDA
- Sponsor
- SUN PHARM
Application Products#
| Product | Drug | Ingredient | Form | Strength | Reference drug | Reference standard |
|---|---|---|---|---|---|---|
| 001 | BUPROPION HYDROCHLORIDE | BUPROPION HYDROCHLORIDE | TABLET, EXTENDED RELEASE;ORAL | 300MG | No | No |
NDC Listings For This Application#
| NDC | Name | Nonproprietary name | Labeler | Marketing category | Status |
|---|---|---|---|---|---|
| 63304-724 | Bupropion hydrochloride | Bupropion hydrochloride | Sun Pharmaceutical Industries, Inc. | ANDA | Current |
| 63304-724 | Bupropion hydrochloride | Bupropion hydrochloride | Sun Pharmaceutical Industries, Inc. | ANDA | Current |
| 63304-724 | Bupropion hydrochloride | Bupropion hydrochloride | Sun Pharmaceutical Industries, Inc. | ANDA | Current |