Home
>
National Drug Code (NDC)
>
Propranolol Hydrochloride
Propranolol Hydrochloride - 0781-3777-95 - (Propranolol Hydrochloride)
Drug Information of Propranolol Hydrochloride
| Product NDC: | 0781-3777 |
| Proprietary Name: | Propranolol Hydrochloride |
| Non Proprietary Name: | Propranolol Hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Propranolol Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propranolol Hydrochloride
| Product NDC: | 0781-3777 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076400 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030226 |
Package Information of Propranolol Hydrochloride
| Package NDC: | 0781-3777-95 |
| Package Description: | 10 VIAL, SINGLE-USE in 1 CARTON (0781-3777-95) > 1 mL in 1 VIAL, SINGLE-USE (0781-3777-71) |
NDC Information of Propranolol Hydrochloride
| NDC Code | 0781-3777-95 |
| Proprietary Name | Propranolol Hydrochloride |
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (0781-3777-95) > 1 mL in 1 VIAL, SINGLE-USE (0781-3777-71) |
| Product NDC | 0781-3777 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propranolol Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20030226 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
