"49348-921-10" National Drug Code (NDC)

Sunmark Arthritis Pain Reliever 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10)
(Sunmark)

NDC Code49348-921-10
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10)
Product NDC49348-921
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Arthritis Pain Reliever
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20020430
Marketing Category NameANDA
Application NumberANDA076200
ManufacturerSunmark
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

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