"70710-1021-1" National Drug Code (NDC)

Albendazole 100 TABLET, FILM COATED in 1 BOTTLE (70710-1021-1)
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1021-1
Package Description100 TABLET, FILM COATED in 1 BOTTLE (70710-1021-1)
Product NDC70710-1021
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlbendazole
Non-Proprietary NameAlbendazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181217
Marketing Category NameANDA
Application NumberANDA208979
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameALBENDAZOLE
Strength200
Strength Unitmg/1
Pharmacy ClassesAnthelmintic [EPC], Cytochrome P450 1A Inducers [MoA]

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