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NDC 78670-003, dantrolene sodium, injection, powder, lyophilized, for solution, from USWM, LLC.

Product NDC
78670-003
Status
Listed
Labeler
USWM, LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078378
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/78670-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DANTROLENE SODIUM20 mg/60mL

Pharmacologic classes

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

Package NDCNDC-11Package
78670-003-67786700003676 VIAL, GLASS in 1 CARTON (78670-003-67) / 60 mL in 1 VIAL, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f1650487-32bd-4017-b9c2-b38829a531af

Use it

Look up 78670-003 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/78670-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 78670-003. 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.