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
- 65862-742_6135c8a8-0232-4aa1-be56-8c29a444d96f
- Product NDC
- 65862-742
- Form
- TABLET, FILM COATED
- Composition / generic term
- Olmesartan Medoxomil
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170424
- Source listing expiry
- 20261231
Source-listed ingredients
- OLMESARTAN MEDOXOMIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-742-01) · 65862-742-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-742-05) · 65862-742-05
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-742-30) · 65862-742-30
- 10 BLISTER PACK in 1 CARTON (65862-742-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-742-10) · 65862-742-78
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-742-90) · 65862-742-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-742-99) · 65862-742-99
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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