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"63739-442-01" National Drug Code (NDC)

Ibu 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-442-01) > 30 TABLET in 1 BLISTER PACK
(McKesson Packaging Services a business unit of McKesson Corporation)

NDC Code63739-442-01
Package Description25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-442-01) > 30 TABLET in 1 BLISTER PACK
Product NDC63739-442
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20090720
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerMcKesson Packaging Services a business unit of McKesson Corporation
Substance NameIBUPROFEN
Strength400
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63739-442-01





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