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"68071-4421-8" National Drug Code (NDC)
Gemfibrozil 180 TABLET in 1 BOTTLE (68071-4421-8)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-4421-8
Package Description
180 TABLET in 1 BOTTLE (68071-4421-8)
Product NDC
68071-4421
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemfibrozil
Non-Proprietary Name
Gemfibrozil
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170215
Marketing Category Name
ANDA
Application Number
ANDA203266
Manufacturer
NuCare Pharmaceuticals,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/68071-4421-8