"61919-312-90" National Drug Code (NDC)

Hydralazine Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (61919-312-90)
(Direct_Rx)

NDC Code61919-312-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61919-312-90)
Product NDC61919-312
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydralazine Hydrochloride
Non-Proprietary NameHydralazine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190813
Marketing Category NameANDA
Application NumberANDA086242
ManufacturerDirect_Rx
Substance NameHYDRALAZINE HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesArteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]

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