FdaApplication
ANDA 207597
Identifiers
- fda_app_no: ANDA207597
Properties
| Property | Value |
|---|---|
| applicant_name | P AND L DEVELOPMENT LLC |
| application_type | ANDA |
| approval_date | 2019-01-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE | DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM | 25MG;220MG | TABLET;ORAL |
1 product