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"49349-296-21" National Drug Code (NDC)
Gemfibrozil 120 TABLET, FILM COATED in 1 CANISTER (49349-296-21)
(REMEDYREPACK INC.)
NDC Code
49349-296-21
Package Description
120 TABLET, FILM COATED in 1 CANISTER (49349-296-21)
Product NDC
49349-296
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemfibrozil
Non-Proprietary Name
Gemfibrozil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110609
Marketing Category Name
ANDA
Application Number
ANDA077836
Manufacturer
REMEDYREPACK INC.
Substance Name
GEMFIBROZIL
Strength
600
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-296-21