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"0093-0771-10" National Drug Code (NDC)
Pravastatin Sodium 1000 TABLET in 1 BOTTLE (0093-0771-10)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-0771-10
Package Description
1000 TABLET in 1 BOTTLE (0093-0771-10)
Product NDC
0093-0771
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20060425
Marketing Category Name
ANDA
Application Number
ANDA076056
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
PRAVASTATIN SODIUM
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/0093-0771-10