"11673-210-62" National Drug Code (NDC)

Up And Up Arthritis Pain Relief 1 BOTTLE in 1 CARTON (11673-210-62) > 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
(Target Corporation)

NDC Code11673-210-62
Package Description1 BOTTLE in 1 CARTON (11673-210-62) > 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC11673-210
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Arthritis Pain Relief
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20150306
End Marketing Date20211130
Marketing Category NameANDA
Application NumberANDA075077
ManufacturerTarget Corporation
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

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