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"67296-1217-2" National Drug Code (NDC)

Ibu 20 TABLET in 1 BOTTLE (67296-1217-2)
(RedPharm Drug, Inc.)

NDC Code67296-1217-2
Package Description20 TABLET in 1 BOTTLE (67296-1217-2)
Product NDC67296-1217
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbu
Dosage FormTABLET
UsageORAL
Start Marketing Date20081120
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerRedPharm Drug, Inc.
Substance NameIBUPROFEN
Strength400
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67296-1217-2





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