"0074-0038-07" National Drug Code (NDC)

Orilissa 1 BLISTER PACK in 1 CARTON (0074-0038-07) / 7 TABLET, FILM COATED in 1 BLISTER PACK
(AbbVie Inc.)

NDC Code0074-0038-07
Package Description1 BLISTER PACK in 1 CARTON (0074-0038-07) / 7 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0074-0038
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOrilissa
Non-Proprietary NameElagolix
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180723
Marketing Category NameNDA
Application NumberNDA210450
ManufacturerAbbVie Inc.
Substance NameELAGOLIX SODIUM
Strength150
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Decreased GnRH Secretion [PE], Gonadotropin Releasing Hormone Receptor Antagonist [EPC], Gonadotropin Releasing Hormone Receptor Antagonists [MoA], P-Glycoprotein Inhibitors [MoA]

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