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"47335-326-18" National Drug Code (NDC)

Naltrexone Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-326-18
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)
Product NDC47335-326
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNaltrexone Hydrochloride
Non-Proprietary NameNaltrexone Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120229
Marketing Category NameANDA
Application NumberANDA090356
ManufacturerSun Pharmaceutical Industries, 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/47335-326-18





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