FdaApplication
ANDA 206151
Identifiers
- fda_app_no: ANDA206151
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA LTD |
| application_type | ANDA |
| approval_date | 2017-03-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ABACAVIR SULFATE AND LAMIVUDINE | ABACAVIR SULFATE; LAMIVUDINE | EQ 600MG BASE;300MG | TABLET;ORAL |
1 product