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
- 71335-2507_97992e54-4553-4e64-97f8-0d04b6ff3133
- Product NDC
- 71335-2507
- Form
- TABLET
- Composition / generic term
- Amlodipine Besylate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180815
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET in 1 BOTTLE (71335-2507-0) · 71335-2507-0
- 30 TABLET in 1 BOTTLE (71335-2507-1) · 71335-2507-1
- 90 TABLET in 1 BOTTLE (71335-2507-2) · 71335-2507-2
- 60 TABLET in 1 BOTTLE (71335-2507-3) · 71335-2507-3
- 120 TABLET in 1 BOTTLE (71335-2507-4) · 71335-2507-4
- 100 TABLET in 1 BOTTLE (71335-2507-5) · 71335-2507-5
- 800 TABLET in 1 BOTTLE (71335-2507-6) · 71335-2507-6
- 1000 TABLET in 1 BOTTLE (71335-2507-7) · 71335-2507-7
- 180 TABLET in 1 BOTTLE (71335-2507-8) · 71335-2507-8
- 10 TABLET in 1 BOTTLE (71335-2507-9) · 71335-2507-9
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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