United States · FDA National Drug Code directory
Olmesartan Medoxomil
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
- 71209-079_c8a58add-6c59-47ff-94e2-12d4e6513feb
- Product NDC
- 71209-079
- Form
- TABLET, COATED
- Composition / generic term
- Olmesartan Medoxomil
- Labeler
- Cadila Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250101
- Source listing expiry
- 20261231
Source-listed ingredients
- OLMESARTAN MEDOXOMIL — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE (71209-079-01) · 71209-079-01
- 90 TABLET, COATED in 1 BOTTLE (71209-079-04) · 71209-079-04
- 500 TABLET, COATED in 1 BOTTLE (71209-079-10) · 71209-079-10
- 1000 TABLET, COATED in 1 BOTTLE (71209-079-11) · 71209-079-11
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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