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Cupric Chloride

NDC 70069-506, Cupric Chloride, injection, from Somerset Therapeutics, LLC.

Product NDC
70069-506
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216113
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-506 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CUPRIC CHLORIDE.4 mg/mL
Package NDCNDC-11Package
70069-506-257006905062525 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/361d30f2-3c97-4a6c-b252-7fa864d0a625

Use it

Look up 70069-506 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-506 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-506. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.