Home
>
National Drug Code (NDC)
>
HYDRALAZINE HYDROCHLORIDE
HYDRALAZINE HYDROCHLORIDE - 21695-679-90 - (Hydralazine Hydrochloride)
Drug Information of HYDRALAZINE HYDROCHLORIDE
| Product NDC: | 21695-679 |
| Proprietary Name: | HYDRALAZINE HYDROCHLORIDE |
| Non Proprietary Name: | Hydralazine Hydrochloride |
| Active Ingredient(s): | 10 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: | 21695-679 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040901 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080912 |
Package Information of HYDRALAZINE HYDROCHLORIDE
| Package NDC: | 21695-679-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (21695-679-90) |
NDC Information of HYDRALAZINE HYDROCHLORIDE
| NDC Code | 21695-679-90 |
| Proprietary Name | HYDRALAZINE HYDROCHLORIDE |
| Package Description | 90 TABLET in 1 BOTTLE (21695-679-90) |
| Product NDC | 21695-679 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydralazine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080912 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
