| NDC Code | 24090-470-88 |
|---|
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24090-470-88) |
|---|
| Product NDC | 24090-470 |
|---|
| 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 | 19830419 |
|---|
| End Marketing Date | 20180131 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA018553 |
|---|
| Manufacturer | Akrimax Pharmaceuticals, LLC |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 60 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|