FdaApplication
NDA 020067
Identifiers
- fda_app_no: NDA020067
Properties
| Property | Value |
|---|---|
| applicant_name | ATNAHS PHARMA US LTD |
| application_type | NDA |
| approval_date | 1994-10-14 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EC-NAPROSYN | NAPROXEN | 500MG | TABLET, DELAYED RELEASE;ORAL |
| EC-NAPROSYN | NAPROXEN | 375MG | TABLET, DELAYED RELEASE;ORAL |
2 products