FdaApplication
ANDA 203694
Identifiers
- fda_app_no: ANDA203694
Properties
| Property | Value |
|---|---|
| applicant_name | MPP PHARMA LLC |
| application_type | ANDA |
| approval_date | 2017-11-30 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 300MG BASE | TABLET;ORAL |
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 150MG BASE | TABLET;ORAL |
2 products