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
- 65841-622_cb1a9e7c-aa86-4596-bc0d-86d8b5750963
- Product NDC
- 65841-622
- Form
- TABLET
- Composition / generic term
- Amlodipine Besylate
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070921
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (65841-622-01) · 65841-622-01
- 500 TABLET in 1 BOTTLE (65841-622-05) · 65841-622-05
- 90 TABLET in 1 BOTTLE (65841-622-16) · 65841-622-16
- 10 BLISTER PACK in 1 CARTON (65841-622-77) / 10 TABLET in 1 BLISTER PACK · 65841-622-77
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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