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: 68788-4049_e6a3d99c-c9cc-49d9-b0f9-503770307b70
Product NDC: 68788-4049
Form: TABLET
Composition / generic term: Pravastatin sodium
Labeler: Preferred Pharmaceuticals Inc.
Marketing category: ANDA
Marketing start / end (source format): 20251031
Source listing expiry: 20261231

Source-listed ingredients

PRAVASTATIN SODIUM — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (68788-4049-3) · 68788-4049-3
60 TABLET in 1 BOTTLE (68788-4049-6) · 68788-4049-6
90 TABLET in 1 BOTTLE (68788-4049-9) · 68788-4049-9

Source and coverage

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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.

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