"63739-672-01" National Drug Code (NDC)

Ibuprofen 25 BLISTER PACK in 1 BOX (63739-672-01) > 30 TABLET in 1 BLISTER PACK
(McKesson Corporation dba SKY Packaging)

NDC Code63739-672-01
Package Description25 BLISTER PACK in 1 BOX (63739-672-01) > 30 TABLET in 1 BLISTER PACK
Product NDC63739-672
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20091123
End Marketing Date20210731
Marketing Category NameANDA
Application NumberANDA078558
ManufacturerMcKesson Corporation dba SKY Packaging
Substance NameIBUPROFEN
Strength400
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

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