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
- 68382-122_cd7a7360-2639-480a-af3d-0cb410c22110
- Product NDC
- 68382-122
- Form
- TABLET
- Composition / generic term
- Amlodipine Besylate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070921
- Source listing expiry
- 20261231
Source-listed ingredients
- AMLODIPINE BESYLATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68382-122-01) · 68382-122-01
- 500 TABLET in 1 BOTTLE (68382-122-05) · 68382-122-05
- 90 TABLET in 1 BOTTLE (68382-122-16) · 68382-122-16
- 10 BLISTER PACK in 1 CARTON (68382-122-77) / 10 TABLET in 1 BLISTER PACK · 68382-122-77
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 →