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"49349-531-02" National Drug Code (NDC)
Lovastatin 30 TABLET in 1 BLISTER PACK (49349-531-02)
(REMEDYREPACK INC.)
NDC Code
49349-531-02
Package Description
30 TABLET in 1 BLISTER PACK (49349-531-02)
Product NDC
49349-531
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20110923
Marketing Category Name
ANDA
Application Number
ANDA075828
Manufacturer
REMEDYREPACK INC.
Substance Name
LOVASTATIN
Strength
40
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/49349-531-02