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"21695-732-30" National Drug Code (NDC)

Gemfibrozil 30 TABLET, FILM COATED in 1 BOTTLE (21695-732-30)
(Rebel Distributors Corp)

NDC Code21695-732-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (21695-732-30)
Product NDC21695-732
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20101109
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerRebel Distributors Corp
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/21695-732-30





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