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
- 68071-1980_56d57f8b-3c6a-be25-e063-6394a90ac109
- Product NDC
- 68071-1980
- Form
- TABLET
- Composition / generic term
- AMLODIPINE BESYLATE
- Labeler
- NuCare Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070926
- Source listing expiry
- 20271231
Source-listed ingredients
- AMLODIPINE BESYLATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (68071-1980-2) · 68071-1980-2
- 30 TABLET in 1 BOTTLE (68071-1980-3) · 68071-1980-3
- 60 TABLET in 1 BOTTLE (68071-1980-6) · 68071-1980-6
- 90 TABLET in 1 BOTTLE (68071-1980-9) · 68071-1980-9
Source and coverage
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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.
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