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"0781-5235-10" National Drug Code (NDC)
Pravastatin Sodium 1000 TABLET in 1 BOTTLE (0781-5235-10)
(Sandoz Inc)
NDC Code
0781-5235-10
Package Description
1000 TABLET in 1 BOTTLE (0781-5235-10)
Product NDC
0781-5235
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140728
Marketing Category Name
ANDA
Application Number
ANDA077491
Manufacturer
Sandoz Inc
Substance Name
PRAVASTATIN SODIUM
Strength
80
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/0781-5235-10