"59368-225-03" National Drug Code (NDC)

Sunmark Pain Reliever 1 BOTTLE in 1 CARTON (59368-225-03) / 50 TABLET in 1 BOTTLE
(Praxis, LLC)

NDC Code59368-225-03
Package Description1 BOTTLE in 1 CARTON (59368-225-03) / 50 TABLET in 1 BOTTLE
Product NDC59368-225
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Pain Reliever
Proprietary Name SuffixExtra Strength
Non-Proprietary NameAcetaminophen
Dosage FormTABLET
UsageORAL
Start Marketing Date20030811
End Marketing Date20250601
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM013
ManufacturerPraxis, LLC
Substance NameACETAMINOPHEN
Strength500
Strength Unitmg/1

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