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Hydralazine Hydrochloride
Hydralazine Hydrochloride - 0615-5649-39 - (Hydralazine Hydrochloride)
Drug Information of Hydralazine Hydrochloride
| Product NDC: | 0615-5649 |
| Proprietary Name: | Hydralazine Hydrochloride |
| Non Proprietary Name: | Hydralazine Hydrochloride |
| Active Ingredient(s): | 100 mg/1 & nbsp; Hydralazine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydralazine Hydrochloride
| Product NDC: | 0615-5649 |
| Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088391 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19830927 |
Package Information of Hydralazine Hydrochloride
| Package NDC: | 0615-5649-39 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (0615-5649-39) |
NDC Information of Hydralazine Hydrochloride
| NDC Code | 0615-5649-39 |
| Proprietary Name | Hydralazine Hydrochloride |
| Package Description | 30 TABLET in 1 BLISTER PACK (0615-5649-39) |
| Product NDC | 0615-5649 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydralazine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19830927 |
| Marketing Category Name | ANDA |
| Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
