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Methocarbamol

NDC 87063-041, Methocarbamol, tablet, film coated, from Asclemed USA, Inc..

Product NDC
87063-041
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213967
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87063-041 \
  -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
87063-041-0187063004101100 TABLET, FILM COATED in 1 BOTTLE (87063-041-01)
87063-041-108706300411010 TABLET, FILM COATED in 1 BOTTLE (87063-041-10)
87063-041-208706300412020 TABLET, FILM COATED in 1 BOTTLE (87063-041-20)
87063-041-308706300413030 TABLET, FILM COATED in 1 BOTTLE (87063-041-30)
87063-041-608706300416060 TABLET, FILM COATED in 1 BOTTLE (87063-041-60)
87063-041-908706300419090 TABLET, FILM COATED in 1 BOTTLE (87063-041-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7f297ac6-a580-4539-a770-fe5d15c2b922

Use it

Look up 87063-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87063-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87063-041. 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.