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"69097-184-15" National Drug Code (NDC)
Pravastatin Sodium 1000 TABLET in 1 BOTTLE (69097-184-15)
(Cipla USA Inc.)
NDC Code
69097-184-15
Package Description
1000 TABLET in 1 BOTTLE (69097-184-15)
Product NDC
69097-184
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20061023
Marketing Category Name
ANDA
Application Number
ANDA077904
Manufacturer
Cipla USA Inc.
Substance Name
PRAVASTATIN SODIUM
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/69097-184-15