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
- 35573-458_f47b85b1-a7d3-437b-a3db-a81e1f1716c4
- Product NDC
- 35573-458
- Form
- CAPSULE
- Composition / generic term
- nicardipine hydrochloride
- Labeler
- Burel Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230108
- Source listing expiry
- 20261231
Source-listed ingredients
- NICARDIPINE HYDROCHLORIDE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE in 1 BOTTLE (35573-458-85) · 35573-458-85
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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