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Metaxalone

NDC 85509-1435, Metaxalone, tablet, from PHOENIX RX LLC.

Product NDC
85509-1435
Status
Listed
Labeler
PHOENIX RX LLC
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/85509-1435 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METAXALONE800 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]

Package NDCNDC-11Package
85509-1435-185509143501120 TABLET in 1 BOTTLE (85509-1435-1)
85509-1435-38550914350330 TABLET in 1 BOTTLE (85509-1435-3)
85509-1435-68550914350660 TABLET in 1 BOTTLE (85509-1435-6)
85509-1435-98550914350990 TABLET in 1 BOTTLE (85509-1435-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/413b300d-4163-afef-e063-6394a90a618f

Use it

Look up 85509-1435 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1435 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85509-1435. 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.