FdaApplication
ANDA 074777
Identifiers
- fda_app_no: ANDA074777
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2005-03-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 25MG BASE/ML | INJECTABLE;INJECTION |
1 product