United States · FDA National Drug Code directory

Pravastatin sodium

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
82868-096_471b4a51-f08f-52a6-e063-6294a90a32d9
Product NDC
82868-096
Form
TABLET
Composition / generic term
Pravastatin sodium
Labeler
Northwind Health Company, LLC
Marketing category
ANDA
Marketing start / end (source format)
20251219
Source listing expiry
20261231

Source-listed ingredients

  • PRAVASTATIN SODIUM — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE, PLASTIC (82868-096-30) · 82868-096-30

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →