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Methocarbamol

NDC 82461-723, Methocarbamol, tablet, film coated, from Medcore LLC.

Product NDC
82461-723
Status
Listed
Labeler
Medcore LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212623
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82461-723 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHOCARBAMOL750 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
82461-723-908246107239090 TABLET, FILM COATED in 1 BOTTLE (82461-723-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1a6b7327-fd42-4de0-bd0d-2dd478502d52

Use it

Look up 82461-723 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82461-723 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82461-723. 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.