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"0093-0670-05" National Drug Code (NDC)
Gemfibrozil 500 TABLET, FILM COATED in 1 BOTTLE (0093-0670-05)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-0670-05
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (0093-0670-05)
Product NDC
0093-0670
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemfibrozil
Non-Proprietary Name
Gemfibrozil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19931124
End Marketing Date
20200331
Marketing Category Name
ANDA
Application Number
ANDA074256
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
GEMFIBROZIL
Strength
600
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/0093-0670-05