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: 68462-198_a6e006b3-4256-4cbb-8ad1-b71f363430cd
Product NDC: 68462-198
Form: TABLET
Composition / generic term: Pravastatin Sodium
Labeler: Glenmark Pharmaceuticals Inc., USA
Marketing category: ANDA
Marketing start / end (source format): 20071228
Source listing expiry: 20261231

Source-listed ingredients

PRAVASTATIN SODIUM — 80 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

500 TABLET in 1 BOTTLE (68462-198-05) · 68462-198-05
90 TABLET in 1 BOTTLE (68462-198-90) · 68462-198-90

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 →