"70710-2159-9" National Drug Code (NDC)

Riociguat 90 TABLET, FILM COATED in 1 BOTTLE (70710-2159-9)
(Zydus Pharmaceuticals USA Inc)

NDC Code70710-2159-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (70710-2159-9)
Product NDC70710-2159
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRiociguat
Non-Proprietary NameRiociguat
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260918
Marketing Category NameANDA
Application NumberANDA211135
ManufacturerZydus Pharmaceuticals USA Inc
Substance NameRIOCIGUAT
Strength2
Strength Unitmg/1
Pharmacy ClassesGuanylate Cyclase Stimulators [MoA], Soluble Guanylate Cyclase Stimulator [EPC]

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