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"71205-169-30" National Drug Code (NDC)

Gemfibrozil 30 TABLET, FILM COATED in 1 BOTTLE (71205-169-30)
(Proficient Rx LP)

NDC Code71205-169-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71205-169-30)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-169-30





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