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"61919-676-71" National Drug Code (NDC)
Lovastatin 100 TABLET in 1 BOTTLE (61919-676-71)
(DIRECT RX)
NDC Code
61919-676-71
Package Description
100 TABLET in 1 BOTTLE (61919-676-71)
Product NDC
61919-676
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160303
Marketing Category Name
ANDA
Application Number
ANDA075636
Manufacturer
DIRECT RX
Substance Name
LOVASTATIN
Strength
20
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/61919-676-71