"70518-1301-0" National Drug Code (NDC)

Gemfibrozil 30 TABLET in 1 BLISTER PACK (70518-1301-0)
(REMEDYREPACK INC.)

NDC Code70518-1301-0
Package Description30 TABLET in 1 BLISTER PACK (70518-1301-0)
Product NDC70518-1301
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20180712
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerREMEDYREPACK INC.
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]

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