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"70518-2887-0" National Drug Code (NDC)
Pravastatin Sodium 90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-0)
(REMEDYREPACK INC.)
NDC Code
70518-2887-0
Package Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-0)
Product NDC
70518-2887
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200915
Marketing Category Name
ANDA
Application Number
ANDA076056
Manufacturer
REMEDYREPACK 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/70518-2887-0