FdaApplication
ANDA 070322
Identifiers
- fda_app_no: ANDA070322
Properties
| Property | Value |
|---|---|
| applicant_name | INNOGENIX LLC |
| application_type | ANDA |
| approval_date | 1985-10-22 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 40MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 60MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 20MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 80MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 10MG | TABLET;ORAL |
5 products