"71205-213-72" National Drug Code (NDC)

Ibuprofen 1 BOTTLE in 1 CARTON (71205-213-72) > 120 mL in 1 BOTTLE
(Proficient Rx LP)

NDC Code71205-213-72
Package Description1 BOTTLE in 1 CARTON (71205-213-72) > 120 mL in 1 BOTTLE
Product NDC71205-213
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormSUSPENSION
UsageORAL
Start Marketing Date20170627
Marketing Category NameANDA
Application NumberANDA209207
ManufacturerProficient Rx LP
Substance NameIBUPROFEN
Strength100
Strength Unitmg/5mL
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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