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SUGAMMADEX SODIUM

NDC 42023-935, SUGAMMADEX SODIUM, solution, from Par Health USA, LLC.

Product NDC
42023-935
Status
Listed
Labeler
Par Health USA, LLC
Dosage form
SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218814
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42023-935 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUGAMMADEX SODIUM500 mg/5mL

Pharmacologic classes

gamma-Cyclodextrins [CS]

Package NDCNDC-11Package
42023-935-104202309351010 SYRINGE in 1 CARTON (42023-935-10) / 5 mL in 1 SYRINGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/579a2a1f-4d0c-4851-e063-6294a90a2be6

Use it

Look up 42023-935 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42023-935 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42023-935. 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.