"71309-111-10" National Drug Code (NDC)

Ibuprofen 200 Mg 1000 BOTTLE in 1 BOTTLE (71309-111-10) > 500 BOTTLE in 1 BOTTLE (71309-111-05) > 30 CARTON in 1 BOTTLE (71309-111-30) > 1 TABLET, COATED in 1 CARTON
(Safrel Pharmaceuticals, LLC.)

NDC Code71309-111-10
Package Description1000 BOTTLE in 1 BOTTLE (71309-111-10) > 500 BOTTLE in 1 BOTTLE (71309-111-05) > 30 CARTON in 1 BOTTLE (71309-111-30) > 1 TABLET, COATED in 1 CARTON
Product NDC71309-111
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen 200 Mg
Non-Proprietary NameIbuprofen
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20110101
Marketing Category NameANDA
Application NumberANDA079174
ManufacturerSafrel Pharmaceuticals, LLC.
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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