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"68788-9668-1" National Drug Code (NDC)
Lovastatin 100 TABLET in 1 BOTTLE (68788-9668-1)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-9668-1
Package Description
100 TABLET in 1 BOTTLE (68788-9668-1)
Product NDC
68788-9668
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130729
Marketing Category Name
ANDA
Application Number
ANDA075991
Manufacturer
Preferred Pharmaceuticals, 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/68788-9668-1