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"70518-2718-0" National Drug Code (NDC)

Naltrexone Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2718-0)
(REMEDYREPACK INC.)

NDC Code70518-2718-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2718-0)
Product NDC70518-2718
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNaltrexone Hydrochloride
Non-Proprietary NameNaltrexone Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200501
Marketing Category NameANDA
Application NumberANDA090356
ManufacturerREMEDYREPACK INC.
Substance NameNALTREXONE HYDROCHLORIDE
Strength50
Strength Unitmg/1
Pharmacy ClassesOpioid Antagonist [EPC],Opioid Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2718-0





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