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Metaxalone

NDC 76420-232, Metaxalone, tablet, from Asclemed USA, Inc..

Product NDC
76420-232
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204770
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METAXALONE800 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE]

Package NDCNDC-11Package
76420-232-207642002322020 TABLET in 1 BOTTLE (76420-232-20)
76420-232-307642002323030 TABLET in 1 BOTTLE (76420-232-30)
76420-232-607642002326060 TABLET in 1 BOTTLE (76420-232-60)
76420-232-907642002329090 TABLET in 1 BOTTLE (76420-232-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/02c42f72-5d78-436d-8105-8c0f8d4c0d91

Use it

Look up 76420-232 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-232. 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.