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"52725-495-07" National Drug Code (NDC)
Fenoglide 6 BOTTLE, PLASTIC in 1 BOX (52725-495-07) > 7 TABLET in 1 BOTTLE, PLASTIC
(Shore Therapeutics, Inc)
NDC Code
52725-495-07
Package Description
6 BOTTLE, PLASTIC in 1 BOX (52725-495-07) > 7 TABLET in 1 BOTTLE, PLASTIC
Product NDC
52725-495
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenoglide
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20101118
Marketing Category Name
NDA
Application Number
NDA022118
Manufacturer
Shore Therapeutics, Inc
Substance Name
FENOFIBRATE
Strength
120
Strength Unit
mg/1
Pharmacy Classes
Peroxisome 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/52725-495-07