FdaApplication
ANDA 075110
Identifiers
- fda_app_no: ANDA075110
Properties
| Property | Value |
|---|---|
| applicant_name | ANI PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 1998-06-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CIMETIDINE HYDROCHLORIDE | CIMETIDINE HYDROCHLORIDE | EQ 300MG BASE/5ML | SOLUTION;ORAL |
1 product