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"71205-522-20" National Drug Code (NDC)

Ibuprofen 20 TABLET, FILM COATED in 1 BOTTLE (71205-522-20)
(Proficient Rx LP)

NDC Code71205-522-20
Package Description20 TABLET, FILM COATED in 1 BOTTLE (71205-522-20)
Product NDC71205-522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180824
Marketing Category NameANDA
Application NumberANDA078329
ManufacturerProficient Rx LP
Substance NameIBUPROFEN
Strength600
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/71205-522-20





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