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Propranolol Hydrochloride
Propranolol Hydrochloride - 52584-003-10 - (Propranolol Hydrochloride)
Drug Information of Propranolol Hydrochloride
| Product NDC: | 52584-003 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propranolol Hydrochloride
| Product NDC: | 52584-003 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075792 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100801 |
Package Information of Propranolol Hydrochloride
| Package NDC: | 52584-003-10 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-003-10) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Propranolol Hydrochloride
| NDC Code | 52584-003-10 |
| Proprietary Name | Propranolol Hydrochloride |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-003-10) > 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 52584-003 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propranolol Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100801 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
