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
- 71335-0473_422f8bd0-f200-4715-8c6d-ed6282eec810
- Product NDC
- 71335-0473
- Form
- TABLET
- Composition / generic term
- AMLODIPINE BESYLATE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070926
- Source listing expiry
- 20271231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET in 1 BOTTLE (71335-0473-0) · 71335-0473-0
- 30 TABLET in 1 BOTTLE (71335-0473-1) · 71335-0473-1
- 90 TABLET in 1 BOTTLE (71335-0473-2) · 71335-0473-2
- 60 TABLET in 1 BOTTLE (71335-0473-3) · 71335-0473-3
- 100 TABLET in 1 BOTTLE (71335-0473-4) · 71335-0473-4
- 180 TABLET in 1 BOTTLE (71335-0473-5) · 71335-0473-5
- 120 TABLET in 1 BOTTLE (71335-0473-6) · 71335-0473-6
- 10 TABLET in 1 BOTTLE (71335-0473-7) · 71335-0473-7
- 500 TABLET in 1 BOTTLE (71335-0473-8) · 71335-0473-8
- 1000 TABLET in 1 BOTTLE (71335-0473-9) · 71335-0473-9
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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