| NDC Code | 68382-522-14 |
|---|
| Package Description | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-522-14) |
|---|
| Product NDC | 68382-522 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propafenone Hydrochloride |
|---|
| Non-Proprietary Name | Propafenone Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220202 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA214184 |
|---|
| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
|---|
| Substance Name | PROPAFENONE HYDROCHLORIDE |
|---|
| Strength | 225 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Antiarrhythmic [EPC] |
|---|