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"51013-811-05" National Drug Code (NDC)

Gemfibrozil 500 TABLET in 1 BOTTLE (51013-811-05)
(PuraCap Pharmaceutical, LLC)

NDC Code51013-811-05
Package Description500 TABLET in 1 BOTTLE (51013-811-05)
Product NDC51013-811
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20180604
Marketing Category NameANDA
Application NumberANDA078012
ManufacturerPuraCap Pharmaceutical, 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/51013-811-05





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