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Succinylcholine Chloride

NDC 71839-121, Succinylcholine Chloride, injection, solution, from BE Pharmaceuticals Inc..

Product NDC
71839-121
Status
Listed
Labeler
BE Pharmaceuticals Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216003
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71839-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUCCINYLCHOLINE CHLORIDE20 mg/mL

Pharmacologic classes

Depolarizing Neuromuscular Blocker [EPC]; Neuromuscular Depolarizing Blockade [PE]

Package NDCNDC-11Package
71839-121-257183901212525 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25) / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6e6e0ce7-c73c-407f-9678-724425f24976

Use it

Look up 71839-121 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71839-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71839-121. 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.