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
59746-466_09a95078-de95-4c58-a910-4cd3b6f04810
Product NDC
59746-466
Form
TABLET, FILM COATED
Composition / generic term
olmesartan medoxomil
Labeler
Jubilant Cadista Pharmacuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20160401
Source listing expiry
20261231

Source-listed ingredients

  • OLMESARTAN MEDOXOMIL — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-466-01) · 59746-466-01
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-466-10) · 59746-466-10
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-466-30) · 59746-466-30
  • 3 BLISTER PACK in 1 CARTON (59746-466-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 59746-466-32
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59746-466-90) · 59746-466-90

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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