NDC 0615-8540

Pravastatin Sodium 20 mg tablet

On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Cipla USA., Inc.'s NDC 69097-789.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals LimitedDhar, IndiaMakes it, tests it, packages it and labels it Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Pravastatin: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA077987
On the market since
Jun 1, 2024
Package NDCs
0615-8540-05 0615-8540-39
Official label
DailyMed (National Library of Medicine), updated Dec 6, 2024

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