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"65841-739-05" National Drug Code (NDC)
Pravastatin Sodium 500 TABLET in 1 BOTTLE (65841-739-05)
(Zydus Lifesciences Limited)
NDC Code
65841-739-05
Package Description
500 TABLET in 1 BOTTLE (65841-739-05)
Product NDC
65841-739
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20100330
Marketing Category Name
ANDA
Application Number
ANDA077751
Manufacturer
Zydus Lifesciences 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/65841-739-05