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"61919-312-90" National Drug Code (NDC)
Hydralazine Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (61919-312-90)
(Direct_Rx)
NDC Code
61919-312-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (61919-312-90)
Product NDC
61919-312
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydralazine Hydrochloride
Non-Proprietary Name
Hydralazine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190813
Marketing Category Name
ANDA
Application Number
ANDA086242
Manufacturer
Direct_Rx
Substance Name
HYDRALAZINE HYDROCHLORIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-312-90