| NDC Code | 62559-522-30 |
|---|
| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-522-30) |
|---|
| Product NDC | 62559-522 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Inderal |
|---|
| Proprietary Name Suffix | La |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170428 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA018553 |
|---|
| Manufacturer | ANI Pharmaceuticals, Inc. |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 120 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
|---|