| NDC Code | 58118-1659-8 |
|---|
| Package Description | 30 TABLET in 1 BLISTER PACK (58118-1659-8) |
|---|
| Product NDC | 58118-1659 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propranolol Hydrochloride |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160919 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA070175 |
|---|
| Manufacturer | Clinical Solutions Wholesale, LLC |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|