FdaApplication
ANDA 040789
Identifiers
- fda_app_no: ANDA040789
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS NY LLC |
| application_type | ANDA |
| approval_date | 2007-11-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 650MG;10MG | TABLET;ORAL |
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 500MG;7.5MG | TABLET;ORAL |
2 products