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dantrolene sodium

NDC 70518-4622, dantrolene sodium, capsule, from REMEDYREPACK INC..

Product NDC
70518-4622
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA017443
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4622 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DANTROLENE SODIUM100 mg/1

Pharmacologic classes

Decreased Striated Muscle Contraction [PE]; Decreased Striated Muscle Tone [PE]; Skeletal Muscle Relaxant [EPC]

Package NDCNDC-11Package
70518-4622-07051846220050 POUCH in 1 BOX (70518-4622-0) / 1 CAPSULE in 1 POUCH (70518-4622-1)
70518-4622-270518462202100 POUCH in 1 BOX (70518-4622-2) / 1 CAPSULE in 1 POUCH (70518-4622-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c10e7eb1-0155-43ff-aa56-8cd468e8e84d

Use it

Look up 70518-4622 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4622 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4622. 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.