FdaApplication
ANDA 075389
Identifiers
- fda_app_no: ANDA075389
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES SA |
| application_type | ANDA |
| approval_date | 2001-01-25 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMIODARONE HYDROCHLORIDE | AMIODARONE HYDROCHLORIDE | 400MG | TABLET;ORAL |
| AMIODARONE HYDROCHLORIDE | AMIODARONE HYDROCHLORIDE | 100MG | TABLET;ORAL |
| AMIODARONE HYDROCHLORIDE | AMIODARONE HYDROCHLORIDE | 200MG | TABLET;ORAL |
3 products