"0051-2638-99" National Drug Code (NDC)

96000 mg in 1 BOTTLE (0051-2638-99)
(AbbVie Inc.)

NDC Code0051-2638-99
Package Description96000 mg in 1 BOTTLE (0051-2638-99)
Product NDC0051-2638
Product Type NameBULK INGREDIENT
Non-Proprietary NameVedolizumab
Dosage FormLIQUID
Start Marketing Date20160929
Marketing Category NameBULK INGREDIENT
ManufacturerAbbVie Inc.
Substance NameVEDOLIZUMAB
Strength96000
Strength Unitmg/96000mg

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