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Propranolol
Propranolol - 63323-604-01 - (PROPRANOLOL HYDROCHLORIDE)
Drug Information of Propranolol
| Product NDC: | 63323-604 |
| Proprietary Name: | Propranolol |
| 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
| Product NDC: | 63323-604 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075826 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010907 |
Package Information of Propranolol
| Package NDC: | 63323-604-01 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-604-01) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Propranolol
| NDC Code | 63323-604-01 |
| Proprietary Name | Propranolol |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-604-01) > 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-604 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROPRANOLOL HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20010907 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
