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: 42708-066_45b3d5c6-5c65-777f-e063-6294a90a58a5
Product NDC: 42708-066
Form: TABLET
Composition / generic term: Amlodipine besylate
Labeler: QPharma Inc
Marketing category: ANDA
Marketing start / end (source format): 20101020
Source listing expiry: 20261231

Source-listed ingredients

AMLODIPINE BESYLATE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (42708-066-30) · 42708-066-30

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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