FdaApplication
ANDA 075262
Identifiers
- fda_app_no: ANDA075262
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS MID ATLANTIC LLC |
| application_type | ANDA |
| approval_date | 1999-03-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 2MG BASE/5ML | SYRUP;ORAL |
1 product