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"16571-784-50" National Drug Code (NDC)

Gemfibrozil 500 TABLET, FILM COATED in 1 BOTTLE (16571-784-50)
(Rising Pharma Holdings, Inc.)

NDC Code16571-784-50
Package Description500 TABLET, FILM COATED in 1 BOTTLE (16571-784-50)
Product NDC16571-784
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150916
Marketing Category NameANDA
Application NumberANDA202726
ManufacturerRising Pharma Holdings, 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/16571-784-50





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