NDC 68462-197

Pravastatin Sodium 40 mg tablet

On the label: Glenmark Pharmaceuticals Inc., USA.

India: 2United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals Inc., USAMonroe, NC, United StatesMakes it Problems found, fixed voluntarilyJun 17, 2025 · 2 inspections, 1 with FDA action
Glenmark Pharmaceuticals LimitedGoa, IndiaMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action
Glenmark Pharmaceuticals LimitedDhar, IndiaMakes it and tests it Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Pravastatin: every company that makes it
Form
tablet, oral
Strength
40 mg
Approval
ANDA ANDA077987
On the market since
May 11, 2007
Package NDCs
68462-197-05 68462-197-90
Official label
DailyMed (National Library of Medicine), updated Jul 8, 2022

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