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"71335-0899-5" National Drug Code (NDC)

Gemfibrozil 180 TABLET, FILM COATED in 1 BOTTLE (71335-0899-5)
(Bryant Ranch Prepack)

NDC Code71335-0899-5
Package Description180 TABLET, FILM COATED in 1 BOTTLE (71335-0899-5)
Product NDC71335-0899
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150916
Marketing Category NameANDA
Application NumberANDA202726
ManufacturerBryant Ranch Prepack
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/71335-0899-5





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