FdaApplication
ANDA 076124
Identifiers
- fda_app_no: ANDA076124
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS MID ATLANTIC LLC |
| application_type | ANDA |
| approval_date | 2007-02-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 15MG BASE/ML | SYRUP;ORAL |
1 product