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"68071-2422-8" National Drug Code (NDC)

Gemfibrozil 180 TABLET in 1 BOTTLE (68071-2422-8)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2422-8
Package Description180 TABLET in 1 BOTTLE (68071-2422-8)
Product NDC68071-2422
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20101220
Marketing Category NameANDA
Application NumberANDA079072
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPPAR alpha [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/68071-2422-8





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