| NDC Code | 60687-237-25 |
|---|
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-237-25) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-237-95) |
|---|
| Product NDC | 60687-237 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propranolol Hydrochloride |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170224 |
|---|
| End Marketing Date | 20181031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078703 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 120 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|