United States · FDA National Drug Code directory
AMLODIPINE AND 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
- 42571-235_2b531912-67b1-6172-e063-6394a90a178f
- Product NDC
- 42571-235
- Form
- TABLET
- Composition / generic term
- Amlodipine and Olmesartan Medoxomil
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180101
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
- OLMESARTAN MEDOXOMIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (42571-235-05) · 42571-235-05
- 1000 TABLET in 1 BOTTLE (42571-235-10) · 42571-235-10
- 30 TABLET in 1 BOTTLE (42571-235-30) · 42571-235-30
- 90 TABLET in 1 BOTTLE (42571-235-90) · 42571-235-90
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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