| NDC | 50228-422-10, 50228-422-30 |
| Set ID | a7ba9184-7dad-4f82-a947-bb2cc6b760ce |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | ScieGen Pharmaceuticals, Inc. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | ANDA211282 |
![FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET [SCIEGEN PHARMACEUTICALS, INC.]](https://medic.hrt.org//dailymed/images/2182/fluoxetine-01.jpg)
![FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET [SCIEGEN PHARMACEUTICALS, INC.]](https://medic.hrt.org//dailymed/images/2182/fluoxetine-02.jpg)
![FLUOXETINE (FLUOXETINE HYDROCHLORIDE) TABLET [SCIEGEN PHARMACEUTICALS, INC.]](https://medic.hrt.org//dailymed/images/2182/fluoxetine-03.jpg)
| NDC | 50228-422-10, 50228-422-30 |
| Set ID | a7ba9184-7dad-4f82-a947-bb2cc6b760ce |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | ScieGen Pharmaceuticals, Inc. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | ANDA211282 |