United States · FDA National Drug Code directory
amlodipine besylate
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
- 59762-2010_4826ff96-be7a-460d-8ec0-d6bd025d1162
- Product NDC
- 59762-2010
- Form
- TABLET
- Composition / generic term
- amlodipine besylate
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20190624
- Source listing expiry
- 20271231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (59762-2010-1) · 59762-2010-1
- 300 TABLET in 1 BOTTLE (59762-2010-3) · 59762-2010-3
- 90 TABLET in 1 BOTTLE (59762-2010-9) · 59762-2010-9
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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