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"71335-0219-3" National Drug Code (NDC)

Sunmark Arthritis 8 Hour 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0219-3)
(Bryant Ranch Prepack)

NDC Code71335-0219-3
Package Description50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0219-3)
Product NDC71335-0219
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Arthritis 8 Hour
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20020430
Marketing Category NameANDA
Application NumberANDA076200
ManufacturerBryant Ranch Prepack
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0219-3





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