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
- 42806-056_ea20d1c2-78a5-4674-b2c2-f74e9fdcdf28
- Product NDC
- 42806-056
- Form
- TABLET
- Composition / generic term
- AMLODIPINE BESYLATE
- Labeler
- Epic Pharma, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110425
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (42806-056-05) · 42806-056-05
- 90 TABLET in 1 BOTTLE (42806-056-09) · 42806-056-09
- 1000 TABLET in 1 BOTTLE (42806-056-10) · 42806-056-10
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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