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HydrALAZINE Hydrochloride
HydrALAZINE Hydrochloride - 64380-734-06 - (HydrALAZINE Hydrochloride)
Drug Information of HydrALAZINE Hydrochloride
| Product NDC: | 64380-734 |
| Proprietary Name: | HydrALAZINE Hydrochloride |
| Non Proprietary Name: | HydrALAZINE Hydrochloride |
| Active Ingredient(s): | 25 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: | 64380-734 |
| Labeler Name: | Strides Arcolab Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200770 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130630 |
Package Information of HydrALAZINE Hydrochloride
| Package NDC: | 64380-734-06 |
| Package Description: | 100 TABLET in 1 BOTTLE (64380-734-06) |
NDC Information of HydrALAZINE Hydrochloride
| NDC Code | 64380-734-06 |
| Proprietary Name | HydrALAZINE Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (64380-734-06) |
| Product NDC | 64380-734 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HydrALAZINE Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130630 |
| Marketing Category Name | ANDA |
| Labeler Name | Strides Arcolab Limited |
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
