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
- 71335-1278_19f9229f-2ed5-4d1a-a854-2fe6a1b10cee
- Product NDC
- 71335-1278
- Form
- TABLET
- Composition / generic term
- Amlodipine besylate
- Labeler
- Bryant Ranch Prepack
- 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
- 5 TABLET in 1 BOTTLE (71335-1278-0) · 71335-1278-0
- 30 TABLET in 1 BOTTLE (71335-1278-1) · 71335-1278-1
- 90 TABLET in 1 BOTTLE (71335-1278-2) · 71335-1278-2
- 60 TABLET in 1 BOTTLE (71335-1278-3) · 71335-1278-3
- 100 TABLET in 1 BOTTLE (71335-1278-4) · 71335-1278-4
- 180 TABLET in 1 BOTTLE (71335-1278-5) · 71335-1278-5
- 120 TABLET in 1 BOTTLE (71335-1278-6) · 71335-1278-6
- 10 TABLET in 1 BOTTLE (71335-1278-7) · 71335-1278-7
- 500 TABLET in 1 BOTTLE (71335-1278-8) · 71335-1278-8
- 1000 TABLET in 1 BOTTLE (71335-1278-9) · 71335-1278-9
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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