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"69097-821-07" National Drug Code (NDC)

Gemfibrozil 100 TABLET in 1 BOTTLE (69097-821-07)
(Cipla USA Inc.)

NDC Code69097-821-07
Package Description100 TABLET in 1 BOTTLE (69097-821-07)
Product NDC69097-821
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20161013
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerCipla USA 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/69097-821-07





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