FdaApplication
ANDA 216663
Identifiers
- fda_app_no: ANDA216663
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2026-01-27 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 80MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 40MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 60MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 10MG | TABLET;ORAL |
| PROPRANOLOL HYDROCHLORIDE | PROPRANOLOL HYDROCHLORIDE | 20MG | TABLET;ORAL |
5 products