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"68001-315-08" National Drug Code (NDC)
Lovastatin 1000 TABLET in 1 BOTTLE (68001-315-08)
(BluePoint Laboratories)
NDC Code
68001-315-08
Package Description
1000 TABLET in 1 BOTTLE (68001-315-08)
Product NDC
68001-315
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071101
Marketing Category Name
ANDA
Application Number
ANDA078296
Manufacturer
BluePoint Laboratories
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/68001-315-08