United States · FDA National Drug Code directory
Nicardipine Hydrochloride
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
- 42806-501_cdaf4385-811f-4e33-9990-b4e2586b81b3
- Product NDC
- 42806-501
- Form
- CAPSULE
- Composition / generic term
- Nicardipine Hydrochloride
- Labeler
- Epic Pharma, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100505
- Source listing expiry
- 20261231
Source-listed ingredients
- NICARDIPINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (42806-501-01) · 42806-501-01
- 500 CAPSULE in 1 BOTTLE (42806-501-05) · 42806-501-05
- 90 CAPSULE in 1 BOTTLE (42806-501-09) · 42806-501-09
- 1000 CAPSULE in 1 BOTTLE (42806-501-10) · 42806-501-10
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 →