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
- 0615-8430_608a3d7a-7d7c-4822-9822-464f0542e505
- Product NDC
- 0615-8430
- Form
- TABLET
- Composition / generic term
- Amlodipine besylate
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101020 / 20261130
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BLISTER PACK (0615-8430-05) · 0615-8430-05
- 7 TABLET in 1 BLISTER PACK (0615-8430-07) · 0615-8430-07
- 28 TABLET in 1 BLISTER PACK (0615-8430-28) · 0615-8430-28
- 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8430-30) / 5 TABLET in 1 BLISTER PACK · 0615-8430-30
- 30 TABLET in 1 BLISTER PACK (0615-8430-39) · 0615-8430-39
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 →