| NDC Code | 71335-0907-4 |
|---|
| Package Description | 18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0907-4) |
|---|
| Product NDC | 71335-0907 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propranolol Hydrochloride |
|---|
| Proprietary Name Suffix | Er |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20171221 |
|---|
| End Marketing Date | 20230531 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA018553 |
|---|
| Manufacturer | Bryant Ranch Prepack |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 120 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
|---|