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
- 51407-951_a6c15fed-d823-4cd4-83fb-2773c4c3f9ce
- Product NDC
- 51407-951
- Form
- TABLET
- Composition / generic term
- Amlodipine Besylate
- Labeler
- GSMS, Incorporated
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070523
- Source listing expiry
- 20271231
Source-listed ingredients
- AMLODIPINE BESYLATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (51407-951-10) · 51407-951-10
- 90 TABLET in 1 BOTTLE (51407-951-90) · 51407-951-90
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 →