FdaApplication
ANDA 206869
Identifiers
- fda_app_no: ANDA206869
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS OF NY LLC |
| application_type | ANDA |
| approval_date | 2017-06-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN | ACETAMINOPHEN; HYDROCODONE BITARTRATE | 300MG;5MG | TABLET;ORAL |
1 product