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"68788-7011-3" National Drug Code (NDC)

Gemfibrozil 30 TABLET in 1 BOTTLE (68788-7011-3)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7011-3
Package Description30 TABLET in 1 BOTTLE (68788-7011-3)
Product NDC68788-7011
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20170828
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerPreferred Pharmaceuticals Inc.
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/68788-7011-3





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