"70710-1022-8" National Drug Code (NDC)

Isotretinoin 3 BLISTER PACK in 1 CARTON (70710-1022-8) / 10 CAPSULE in 1 BLISTER PACK
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1022-8
Package Description3 BLISTER PACK in 1 CARTON (70710-1022-8) / 10 CAPSULE in 1 BLISTER PACK
Product NDC70710-1022
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIsotretinoin
Non-Proprietary NameIsotretinoin
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20230912
Marketing Category NameANDA
Application NumberANDA211568
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameISOTRETINOIN
Strength10
Strength Unitmg/1
Pharmacy ClassesRetinoid [EPC], Retinoids [CS]

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