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"61786-850-19" National Drug Code (NDC)

Gemfibrozil 90 TABLET in 1 BOTTLE, PLASTIC (61786-850-19)
(REMEDYREPACK INC.)

NDC Code61786-850-19
Package Description90 TABLET in 1 BOTTLE, PLASTIC (61786-850-19)
Product NDC61786-850
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20160831
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerREMEDYREPACK INC.
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61786-850-19





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