FdaApplication
ANDA 211499
Identifiers
- fda_app_no: ANDA211499
Properties
| Property | Value |
|---|---|
| applicant_name | ABHAI LLC |
| application_type | ANDA |
| approval_date | 2018-12-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 325MG/5ML;5MG/5ML | SOLUTION;ORAL |
1 product