FdaApplication
ANDA 216462
Identifiers
- fda_app_no: ANDA216462
Properties
| Property | Value |
|---|---|
| applicant_name | GLENMARK PHARMACEUTICALS LTD |
| application_type | ANDA |
| approval_date | 2022-11-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM PHENYLBUTYRATE | SODIUM PHENYLBUTYRATE | 500MG | TABLET;ORAL |
1 product