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Propranolol Hydrochloride
Propranolol Hydrochloride - 68084-503-01 - (propranolol hydrochloride)
Drug Information of Propranolol Hydrochloride
| Product NDC: | 68084-503 |
| Proprietary Name: | Propranolol Hydrochloride |
| Non Proprietary Name: | propranolol hydrochloride |
| Active Ingredient(s): | 60 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: | 68084-503 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018553 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130705 |
Package Information of Propranolol Hydrochloride
| Package NDC: | 68084-503-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-503-01) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-503-11) |
NDC Information of Propranolol Hydrochloride
| NDC Code | 68084-503-01 |
| Proprietary Name | Propranolol Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-503-01) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-503-11) |
| Product NDC | 68084-503 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | propranolol hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130705 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | American Health Packaging |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
