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"0615-3559-31" National Drug Code (NDC)

Gemfibrozil 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-3559-31)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-3559-31
Package Description31 TABLET, FILM COATED in 1 BLISTER PACK (0615-3559-31)
Product NDC0615-3559
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19931124
Marketing Category NameANDA
Application NumberANDA074256
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0615-3559-31





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