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Propranolol
Propranolol - 0143-9872-01 - (Propranolol)
Drug Information of Propranolol
| Product NDC: | 0143-9872 |
| Proprietary Name: | Propranolol |
| Non Proprietary Name: | Propranolol |
| Active Ingredient(s): | 1 mg/mL & nbsp; Propranolol |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propranolol
| Product NDC: | 0143-9872 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077760 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080131 |
Package Information of Propranolol
| Package NDC: | 0143-9872-01 |
| Package Description: | 1 mL in 1 VIAL (0143-9872-01) |
NDC Information of Propranolol
| NDC Code | 0143-9872-01 |
| Proprietary Name | Propranolol |
| Package Description | 1 mL in 1 VIAL (0143-9872-01) |
| Product NDC | 0143-9872 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propranolol |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080131 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
