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"70518-4764-0" National Drug Code (NDC)

Gemfibrozil 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4764-0)
(REMEDYREPACK INC.)

NDC Code70518-4764-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4764-0)
Product NDC70518-4764
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260924
Marketing Category NameANDA
Application NumberANDA202726
ManufacturerREMEDYREPACK INC.
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesFibric Acids [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/70518-4764-0





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