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sugammadex

NDC 68462-695, sugammadex, injection, solution, from GLENMARK PHARMACEUTICALS INC., USA.

Product NDC
68462-695
Status
Listed
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214364
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-695 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUGAMMADEX SODIUM200 mg/2mL

Pharmacologic classes

gamma-Cyclodextrins [CS]

Package NDCNDC-11Package
68462-695-206846206952010 VIAL, SINGLE-DOSE in 1 CARTON (68462-695-20) / 2 mL in 1 VIAL, SINGLE-DOSE (68462-695-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e7897fc1-4553-460c-a29b-0bc91cd9ca10

Use it

Look up 68462-695 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-695 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-695. 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.