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"70518-4305-0" National Drug Code (NDC)

Gemfibrozil 180 TABLET in 1 BOTTLE, PLASTIC (70518-4305-0)
(REMEDYREPACK INC.)

NDC Code70518-4305-0
Package Description180 TABLET in 1 BOTTLE, PLASTIC (70518-4305-0)
Product NDC70518-4305
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20250309
Marketing Category NameANDA
Application NumberANDA214603
ManufacturerREMEDYREPACK INC.
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/70518-4305-0





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