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
- 16729-010_438f9112-0851-75e1-e063-6294a90a675c
- Product NDC
- 16729-010
- Form
- TABLET
- Composition / generic term
- PRAVASTATIN SODIUM
- Labeler
- Accord Healthcare Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170216
- Source listing expiry
- 20261231
Source-listed ingredients
- PRAVASTATIN SODIUM — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (16729-010-15) · 16729-010-15
- 500 TABLET in 1 BOTTLE (16729-010-16) · 16729-010-16
- 1000 TABLET in 1 BOTTLE (16729-010-17) · 16729-010-17
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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