"49349-296-21" National Drug Code (NDC)

Gemfibrozil 120 TABLET, FILM COATED in 1 CANISTER (49349-296-21)
(REMEDYREPACK INC.)

NDC Code49349-296-21
Package Description120 TABLET, FILM COATED in 1 CANISTER (49349-296-21)
Product NDC49349-296
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110609
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]

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