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"71335-1902-4" National Drug Code (NDC)

Gemfibrozil 90 TABLET in 1 BOTTLE (71335-1902-4)
(Bryant Ranch Prepack)

NDC Code71335-1902-4
Package Description90 TABLET in 1 BOTTLE (71335-1902-4)
Product NDC71335-1902
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20170215
Marketing Category NameANDA
Application NumberANDA203266
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/71335-1902-4





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