FdaApplication
ANDA 217780
Identifiers
- fda_app_no: ANDA217780
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMAZONE |
| application_type | ANDA |
| approval_date | 2023-08-21 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GUAIFENESIN | GUAIFENESIN | 600MG | TABLET, EXTENDED RELEASE;ORAL |
| GUAIFENESIN | GUAIFENESIN | 1.2GM | TABLET, EXTENDED RELEASE;ORAL |
2 products