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"70518-1301-0" National Drug Code (NDC)
Gemfibrozil 30 TABLET in 1 BLISTER PACK (70518-1301-0)
(REMEDYREPACK INC.)
NDC Code
70518-1301-0
Package Description
30 TABLET in 1 BLISTER PACK (70518-1301-0)
Product NDC
70518-1301
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemfibrozil
Non-Proprietary Name
Gemfibrozil
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180712
Marketing Category Name
ANDA
Application Number
ANDA077836
Manufacturer
REMEDYREPACK 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/70518-1301-0