FdaApplication
ANDA 074916
Identifiers
- fda_app_no: ANDA074916
Properties
| Property | Value |
|---|---|
| applicant_name | P AND L DEVELOPMENT LLC |
| application_type | ANDA |
| approval_date | 1999-04-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 100MG/5ML | SUSPENSION;ORAL |
1 product