"63739-691-10" National Drug Code (NDC)

Ibuprofen 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-691-10) > 10 TABLET in 1 BLISTER PACK
(McKesson Corporation dba SKY Packaging)

NDC Code63739-691-10
Package Description10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-691-10) > 10 TABLET in 1 BLISTER PACK
Product NDC63739-691
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
Strength800
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

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