FdaApplication
ANDA 209008
Identifiers
- fda_app_no: ANDA209008
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA LTD |
| application_type | ANDA |
| approval_date | 2017-06-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PSEUDOEPHEDRINE HYDROCHLORIDE | PSEUDOEPHEDRINE HYDROCHLORIDE | 120MG | TABLET, EXTENDED RELEASE;ORAL |
1 product