"50580-112-37" National Drug Code (NDC)

Tylenol Arthritis Pain 1 BOTTLE in 1 CARTON (50580-112-37) > 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
(McNeil Consumer Healthcare Div McNeil-PPC, Inc)

NDC Code50580-112-37
Package Description1 BOTTLE in 1 CARTON (50580-112-37) > 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC50580-112
Product Type NameHUMAN OTC DRUG
Proprietary NameTylenol Arthritis Pain
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date19981201
Marketing Category NameNDA
Application NumberNDA019872
ManufacturerMcNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

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