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Sugammadex

NDC 70710-1651, Sugammadex, injection, solution, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1651
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214290
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1651 \
  -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
70710-1651-67071016510610 VIAL, SINGLE-DOSE in 1 CARTON (70710-1651-6) / 5 mL in 1 VIAL, SINGLE-DOSE (70710-1651-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/21028965-598b-4cfa-a614-5c28ed40306a

Use it

Look up 70710-1651 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1651 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1651. 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.