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
50090-6853_a133e010-5957-430e-b449-aae85224caab
Product NDC
50090-6853
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 — 2.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (50090-6853-0) · 50090-6853-0

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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