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
- 71335-0833_c9d18f34-5d9f-4f67-afbd-d28b28cbe15e
- Product NDC
- 71335-0833
- Form
- TABLET
- Composition / generic term
- Amlodipine besylate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071102
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 2.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-0833-1) · 71335-0833-1
- 90 TABLET in 1 BOTTLE (71335-0833-2) · 71335-0833-2
- 120 TABLET in 1 BOTTLE (71335-0833-3) · 71335-0833-3
- 60 TABLET in 1 BOTTLE (71335-0833-4) · 71335-0833-4
- 500 TABLET in 1 BOTTLE (71335-0833-5) · 71335-0833-5
- 10 TABLET in 1 BOTTLE (71335-0833-6) · 71335-0833-6
- 100 TABLET in 1 BOTTLE (71335-0833-7) · 71335-0833-7
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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