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"52125-718-02" National Drug Code (NDC)
Lovastatin 30 TABLET in 1 BLISTER PACK (52125-718-02)
(REMEDYREPACK INC.)
NDC Code
52125-718-02
Package Description
30 TABLET in 1 BLISTER PACK (52125-718-02)
Product NDC
52125-718
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130927
Marketing Category Name
ANDA
Application Number
ANDA075828
Manufacturer
REMEDYREPACK INC.
Substance Name
LOVASTATIN
Strength
10
Strength Unit
mg/1
Pharmacy Classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-718-02