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
- 71610-620_1490fc40-2c20-dd29-e063-6294a90aed09
- Product NDC
- 71610-620
- Form
- TABLET
- Composition / generic term
- AMLODIPINE BESYLATE
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110425
- 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 (71610-620-30) · 71610-620-30
- 35 TABLET in 1 BOTTLE (71610-620-35) · 71610-620-35
- 45 TABLET in 1 BOTTLE (71610-620-45) · 71610-620-45
- 90 TABLET in 1 BOTTLE (71610-620-60) · 71610-620-60
- 180 TABLET in 1 BOTTLE (71610-620-80) · 71610-620-80
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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