FdaApplication
ANDA 074252
Identifiers
- fda_app_no: ANDA074252
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PARENTERAL MEDICINES INC |
| application_type | ANDA |
| approval_date | 1997-11-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CIMETIDINE HYDROCHLORIDE | CIMETIDINE HYDROCHLORIDE | EQ 300MG BASE/2ML | INJECTABLE;INJECTION |
1 product