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Metaxalone

NDC 71205-016, Metaxalone, tablet, from Proficient Rx LP.

Product NDC
71205-016
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207466
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-016 \
  -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
71205-016-107120500161010 TABLET in 1 BOTTLE (71205-016-10)
71205-016-307120500163030 TABLET in 1 BOTTLE (71205-016-30)
71205-016-607120500166060 TABLET in 1 BOTTLE (71205-016-60)
71205-016-907120500169090 TABLET in 1 BOTTLE (71205-016-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9c7d0cd4-625a-485e-9d13-ce854630148c

Use it

Look up 71205-016 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-016 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-016. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.