| NDC Code | 17856-3728-1 |
|---|
| Package Description | 72 CUP in 1 CASE (17856-3728-1) / 5 mL in 1 CUP |
|---|
| Product NDC | 17856-3728 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propranolol Hydrochloride |
|---|
| Non-Proprietary Name | Propranolol Hydrochloride |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19870515 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA070979 |
|---|
| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
|---|
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
|---|