FdaApplication
ANDA 207684
Identifiers
- fda_app_no: ANDA207684
Properties
| Property | Value |
|---|---|
| applicant_name | CIPLA LTD |
| application_type | ANDA |
| approval_date | 2017-08-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NEVIRAPINE | NEVIRAPINE | 50MG/5ML | SUSPENSION;ORAL |
1 product