"49348-706-01" National Drug Code (NDC)

Sunmark Ibuprofen 1 BOTTLE in 1 CARTON (49348-706-01) > 10 TABLET, FILM COATED in 1 BOTTLE
(McKesson)

NDC Code49348-706-01
Package Description1 BOTTLE in 1 CARTON (49348-706-01) > 10 TABLET, FILM COATED in 1 BOTTLE
Product NDC49348-706
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Ibuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20030624
Marketing Category NameANDA
Application NumberANDA072096
ManufacturerMcKesson
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1

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