FdaApplication
ANDA 078890
Identifiers
- fda_app_no: ANDA078890
Properties
| Property | Value |
|---|---|
| applicant_name | LANNETT CO INC |
| application_type | ANDA |
| approval_date | 2010-07-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RANITIDINE HYDROCHLORIDE | RANITIDINE HYDROCHLORIDE | EQ 15MG BASE/ML | SYRUP;ORAL |
1 product