"11673-835-06" National Drug Code (NDC)

Up And Up Ibuprofen Sodium 1 BOTTLE in 1 CARTON (11673-835-06) > 160 TABLET, FILM COATED in 1 BOTTLE
(Target Corporation)

NDC Code11673-835-06
Package Description1 BOTTLE in 1 CARTON (11673-835-06) > 160 TABLET, FILM COATED in 1 BOTTLE
Product NDC11673-835
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Ibuprofen Sodium
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170302
Marketing Category NameANDA
Application NumberANDA206581
ManufacturerTarget Corporation
Substance NameIBUPROFEN SODIUM
Strength256
Strength Unitmg/1

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