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"49349-982-19" National Drug Code (NDC)
Lovastatin 90 TABLET in 1 BOTTLE (49349-982-19)
(REMEDYREPACK INC.)
NDC Code
49349-982-19
Package Description
90 TABLET in 1 BOTTLE (49349-982-19)
Product NDC
49349-982
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20131105
Marketing Category Name
ANDA
Application Number
ANDA075991
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/49349-982-19