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Methocarbamol Tablets, USP, 500 mg

NDC 63561-0173, Methocarbamol, tablet, film coated, from Granulation Technology, Inc..

Product NDC
63561-0173
Status
Listed
Labeler
Granulation Technology, Inc.
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/63561-0173 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHOCARBAMOL500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
63561-0173-163561017301100 TABLET, FILM COATED in 1 BOTTLE (63561-0173-1)
63561-0173-563561017305500 TABLET, FILM COATED in 1 BOTTLE (63561-0173-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/70c5342c-9597-4fe6-863c-f8ae4adc063a

  • NADAC price for package 63561017301

    GET /v1/drugs/nadac/63561017301

  • NADAC price for package 63561017305

    GET /v1/drugs/nadac/63561017305

Use it

Look up 63561-0173 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0173 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63561-0173. 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.