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Succinylcholine Chloride

NDC 70069-301, Succinylcholine Chloride, injection, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-301
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211589
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-301 \
  -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
70069-301-107006903011010 VIAL in 1 CARTON (70069-301-10) / 10 mL in 1 VIAL (70069-301-01)
70069-301-257006903012525 VIAL in 1 CARTON (70069-301-25) / 10 mL in 1 VIAL (70069-301-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/499a4ba0-d466-4342-88da-9f1eb6098692

Use it

Look up 70069-301 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-301 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-301. 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.