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"68788-7056-3" National Drug Code (NDC)
Lovastatin 30 TABLET in 1 BOTTLE (68788-7056-3)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7056-3
Package Description
30 TABLET in 1 BOTTLE (68788-7056-3)
Product NDC
68788-7056
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lovastatin
Non-Proprietary Name
Lovastatin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180105
Marketing Category Name
ANDA
Application Number
ANDA075991
Manufacturer
Preferred Pharmaceuticals Inc.
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/68788-7056-3