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"55111-229-01" National Drug Code (NDC)
Pravastatin Sodium 100 TABLET in 1 BOTTLE (55111-229-01)
(Dr.Reddy's Laboratories Limited)
NDC Code
55111-229-01
Package Description
100 TABLET in 1 BOTTLE (55111-229-01)
Product NDC
55111-229
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20091231
Marketing Category Name
ANDA
Application Number
ANDA076714
Manufacturer
Dr.Reddy's Laboratories Limited
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/55111-229-01