FdaApplication
ANDA 206729
Identifiers
- fda_app_no: ANDA206729
Properties
| Property | Value |
|---|---|
| applicant_name | MICRO LABS LTD |
| application_type | ANDA |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NEBIVOLOL HYDROCHLORIDE | NEBIVOLOL HYDROCHLORIDE | 2.5MG | TABLET;ORAL |
| NEBIVOLOL HYDROCHLORIDE | NEBIVOLOL HYDROCHLORIDE | 20MG | TABLET;ORAL |
| NEBIVOLOL HYDROCHLORIDE | NEBIVOLOL HYDROCHLORIDE | 10MG | TABLET;ORAL |
| NEBIVOLOL HYDROCHLORIDE | NEBIVOLOL HYDROCHLORIDE | 5MG | TABLET;ORAL |
4 products