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
- 82432-103_434901d7-2140-d6d8-e063-6394a90a07c4
- Product NDC
- 82432-103
- Form
- INJECTION
- Composition / generic term
- Nicardipine Hydrochloride
- Labeler
- Chengdu Shuode Pharmaceutical Co., Ltd
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240911
- Source listing expiry
- 20261231
Source-listed ingredients
- NICARDIPINE HYDROCHLORIDE — 25 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (82432-103-01) / 10 mL in 1 VIAL, GLASS · 82432-103-01
- 10 VIAL, GLASS in 1 CARTON (82432-103-02) / 10 mL in 1 VIAL, GLASS · 82432-103-02
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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