"68071-2156-3" National Drug Code (NDC)

Naltrexone Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (68071-2156-3)
(NuCare Pharmaceuticls, Inc.)

NDC Code68071-2156-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-2156-3)
Product NDC68071-2156
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNaltrexone Hydrochloride
Non-Proprietary NameNaltrexone Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130923
Marketing Category NameANDA
Application NumberANDA075274
ManufacturerNuCare Pharmaceuticls, Inc.
Substance NameNALTREXONE HYDROCHLORIDE
Strength50
Strength Unitmg/1
Pharmacy ClassesOpioid Antagonist [EPC],Opioid Antagonists [MoA]

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