"0093-0670-05" National Drug Code (NDC)

Gemfibrozil 500 TABLET, FILM COATED in 1 BOTTLE (0093-0670-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-0670-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0093-0670-05)
Product NDC0093-0670
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19931124
End Marketing Date20200331
Marketing Category NameANDA
Application NumberANDA074256
ManufacturerTeva Pharmaceuticals USA, 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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