FdaApplication
ANDA 217000
Identifiers
- fda_app_no: ANDA217000
Properties
| Property | Value |
|---|---|
| applicant_name | BIONPHARMA INC |
| application_type | ANDA |
| approval_date | 2023-08-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE | DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE | 10MG;10MG | TABLET, DELAYED RELEASE;ORAL |
1 product