"51672-4108-8" National Drug Code (NDC)

Ondansetron Hydrochloride 1 BLISTER PACK in 1 CARTON (51672-4108-8) > 3 TABLET, FILM COATED in 1 BLISTER PACK
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-4108-8
Package Description1 BLISTER PACK in 1 CARTON (51672-4108-8) > 3 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC51672-4108
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110328
Marketing Category NameANDA
Application NumberANDA077729
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

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