FdaApplication
ANDA 211890
Identifiers
- fda_app_no: ANDA211890
Properties
| Property | Value |
|---|---|
| applicant_name | ALKEM LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2021-08-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN AND FAMOTIDINE | FAMOTIDINE; IBUPROFEN | 26.6MG;800MG | TABLET;ORAL |
1 product