FdaApplication
ANDA 206891
Identifiers
- fda_app_no: ANDA206891
Properties
| Property | Value |
|---|---|
| applicant_name | ACELLA PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2017-06-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROCODONE BITARTRATE AND CHLORPHENIRAMINE MALEATE | CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE | 4MG/5ML;5MG/5ML | SOLUTION;ORAL |
1 product