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
- 71335-3126_2abdb000-40fa-48e8-8e70-c4ebd885d810
- Product NDC
- 71335-3126
- Form
- TABLET
- Composition / generic term
- Amlodipine besylate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251206
- Source listing expiry
- 20271231
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 (71335-3126-1) · 71335-3126-1
- 90 TABLET in 1 BOTTLE (71335-3126-2) · 71335-3126-2
- 120 TABLET in 1 BOTTLE (71335-3126-3) · 71335-3126-3
- 60 TABLET in 1 BOTTLE (71335-3126-4) · 71335-3126-4
- 500 TABLET in 1 BOTTLE (71335-3126-5) · 71335-3126-5
- 10 TABLET in 1 BOTTLE (71335-3126-6) · 71335-3126-6
- 100 TABLET in 1 BOTTLE (71335-3126-7) · 71335-3126-7
- 180 TABLET in 1 BOTTLE (71335-3126-8) · 71335-3126-8
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →