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Propranolol Hydrochloride
Propranolol Hydrochloride - 0615-2562-39 - (Propranolol Hydrochloride)
Drug Information of Propranolol Hydrochloride
| Product NDC: | 0615-2562 |
| Proprietary Name: | Propranolol Hydrochloride |
| Non Proprietary Name: | Propranolol Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Propranolol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propranolol Hydrochloride
| Product NDC: | 0615-2562 |
| Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070213 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19851119 |
Package Information of Propranolol Hydrochloride
| Package NDC: | 0615-2562-39 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (0615-2562-39) |
NDC Information of Propranolol Hydrochloride
| NDC Code | 0615-2562-39 |
| Proprietary Name | Propranolol Hydrochloride |
| Package Description | 30 TABLET in 1 BLISTER PACK (0615-2562-39) |
| Product NDC | 0615-2562 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propranolol Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19851119 |
| Marketing Category Name | ANDA |
| Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
