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Propranolol Hydrochloride
Propranolol Hydrochloride - 43478-902-88 - (propranolol hydrochloride)
Drug Information of Propranolol Hydrochloride
| Product NDC: | 43478-902 |
| Proprietary Name: | Propranolol Hydrochloride |
| Non Proprietary Name: | propranolol hydrochloride |
| Active Ingredient(s): | 120 mg/1 & nbsp; propranolol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propranolol Hydrochloride
| Product NDC: | 43478-902 |
| Labeler Name: | Rouses Point Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018553 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19830419 |
Package Information of Propranolol Hydrochloride
| Package NDC: | 43478-902-88 |
| Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43478-902-88) |
NDC Information of Propranolol Hydrochloride
| NDC Code | 43478-902-88 |
| Proprietary Name | Propranolol Hydrochloride |
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43478-902-88) |
| Product NDC | 43478-902 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | propranolol hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19830419 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Rouses Point Pharmaceuticals, LLC |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
