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"68001-213-00" National Drug Code (NDC)
Lovastatin 100 TABLET in 1 BOTTLE (68001-213-00)
(BluePoint Laboratories)
NDC Code
68001-213-00
Package Description
100 TABLET in 1 BOTTLE (68001-213-00)
Product NDC
68001-213
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140210
End Marketing Date
20181031
Marketing Category Name
ANDA
Application Number
ANDA075636
Manufacturer
BluePoint Laboratories
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/68001-213-00