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"70518-1710-0" National Drug Code (NDC)
Pravastatin Sodium 90 TABLET in 1 BOTTLE, PLASTIC (70518-1710-0)
(REMEDYREPACK INC.)
NDC Code
70518-1710-0
Package Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-1710-0)
Product NDC
70518-1710
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20181205
Marketing Category Name
ANDA
Application Number
ANDA207068
Manufacturer
REMEDYREPACK 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/70518-1710-0