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
- 68071-4251_1a3c688f-f39c-24be-e063-6394a90a617c
- Product NDC
- 68071-4251
- Form
- TABLET
- Composition / generic term
- Amlodipine besylate
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 120 TABLET in 1 BOTTLE (68071-4251-1) · 68071-4251-1
- 30 TABLET in 1 BOTTLE (68071-4251-3) · 68071-4251-3
- 60 TABLET in 1 BOTTLE (68071-4251-6) · 68071-4251-6
- 90 TABLET in 1 BOTTLE (68071-4251-9) · 68071-4251-9
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 →