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
- 50090-2581_ac5a7515-6873-4ec9-ac86-a6b3cc95b7ba
- Product NDC
- 50090-2581
- Form
- TABLET
- Composition / generic term
- Amlodipine besylate
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101020
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (50090-2581-0) · 50090-2581-0
- 90 TABLET in 1 BOTTLE (50090-2581-1) · 50090-2581-1
- 100 TABLET in 1 BOTTLE (50090-2581-2) · 50090-2581-2
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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