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
- 70069-876_035cb7ef-c5d5-4752-8d43-61b8e8420330
- Product NDC
- 70069-876
- Form
- INJECTION
- Composition / generic term
- Nicardipine Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260420
- Source listing expiry
- 20271231
Source-listed ingredients
- NICARDIPINE HYDROCHLORIDE — .2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 POUCH in 1 CASE (70069-876-10) / 1 BAG in 1 POUCH (70069-876-01) / 200 mL in 1 BAG · 70069-876-10
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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