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"51138-588-30" National Drug Code (NDC)

Gemfibrozil 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-588-30)
(Med-Health Pharma, LLC)

NDC Code51138-588-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-588-30)
Product NDC51138-588
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110704
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerMed-Health Pharma, LLC
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/51138-588-30





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