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Methocarbamol

NDC 87063-135, methocarbamol, tablet, from ASCLEMED USA INC..

Product NDC
87063-135
Status
Listed
Labeler
ASCLEMED USA INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040489
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87063-135 \
  -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
87063-135-0187063013501100 TABLET in 1 BOTTLE (87063-135-01)
87063-135-148706301351414 TABLET in 1 BOTTLE (87063-135-14)
87063-135-308706301353030 TABLET in 1 BOTTLE (87063-135-30)
87063-135-608706301356060 TABLET in 1 BOTTLE (87063-135-60)
87063-135-908706301359090 TABLET in 1 BOTTLE (87063-135-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/077fa923-bee0-4b34-a52d-6f870bcb4828

Use it

Look up 87063-135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87063-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87063-135. 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.