"71205-169-90" National Drug Code (NDC)

Gemfibrozil 90 TABLET, FILM COATED in 1 BOTTLE (71205-169-90)
(Proficient Rx LP)

NDC Code71205-169-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (71205-169-90)
Product NDC71205-169
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150916
Marketing Category NameANDA
Application NumberANDA202726
ManufacturerProficient Rx LP
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]

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