FdaApplication
ANDA 071264
Identifiers
- fda_app_no: ANDA071264
Properties
| Property | Value |
|---|---|
| applicant_name | ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV |
| application_type | ANDA |
| approval_date | 1986-07-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 800MG | TABLET;ORAL |
1 product