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
- 67877-902_700631a3-7f24-4699-a195-0a6a7fae214e
- Product NDC
- 67877-902
- Form
- TABLET
- Composition / generic term
- Amlodipine besylate
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251206
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (67877-902-05) · 67877-902-05
- 1000 TABLET in 1 BOTTLE (67877-902-10) · 67877-902-10
- 90 TABLET in 1 BOTTLE (67877-902-90) · 67877-902-90
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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