FdaApplication
ANDA 074764
Identifiers
- fda_app_no: ANDA074764
Properties
| Property | Value |
|---|---|
| applicant_name | BEDFORD LABORATORIES DIV BEN VENUE LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2004-11-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 25MG BASE/ML | INJECTABLE;INJECTION |
1 product