FdaApplication
ANDA 216800
Identifiers
- fda_app_no: ANDA216800
Properties
| Property | Value |
|---|---|
| applicant_name | ANNORA PHARMA PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2023-05-31 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUPROPION HYDROCHLORIDE | BUPROPION HYDROCHLORIDE | 150MG | TABLET, EXTENDED RELEASE;ORAL |
| BUPROPION HYDROCHLORIDE | BUPROPION HYDROCHLORIDE | 100MG | TABLET, EXTENDED RELEASE;ORAL |
| BUPROPION HYDROCHLORIDE | BUPROPION HYDROCHLORIDE | 200MG | TABLET, EXTENDED RELEASE;ORAL |
3 products