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
- 65862-102_7929af8c-f3da-4b86-8388-20bbe247336e
- Product NDC
- 65862-102
- Form
- TABLET
- Composition / generic term
- Amlodipine Besylate
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070717
- Source listing expiry
- 20271231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (65862-102-05) · 65862-102-05
- 30 TABLET in 1 BOTTLE (65862-102-30) · 65862-102-30
- 90 TABLET in 1 BOTTLE (65862-102-90) · 65862-102-90
- 1000 TABLET in 1 BOTTLE (65862-102-99) · 65862-102-99
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 →