"50580-670-30" National Drug Code (NDC)

Sudafed 12 Hour 3 CARTON in 1 PACKAGE (50580-670-30) > 1 BLISTER PACK in 1 CARTON (50580-670-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
(Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)

NDC Code50580-670-30
Package Description3 CARTON in 1 PACKAGE (50580-670-30) > 1 BLISTER PACK in 1 CARTON (50580-670-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC50580-670
Product Type NameHUMAN OTC DRUG
Proprietary NameSudafed 12 Hour
Non-Proprietary NamePseudoephedrine Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20080601
Marketing Category NameANDA
Application NumberANDA073585
ManufacturerJohnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
Substance NamePSEUDOEPHEDRINE HYDROCHLORIDE
Strength120
Strength Unitmg/1

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