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Methocarbamol

NDC 76420-040, Methocarbamol, tablet, film coated, from Asclemed USA, Inc..

Product NDC
76420-040
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208507
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-040 \
  -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
76420-040-307642000403030 TABLET, FILM COATED in 1 BOTTLE (76420-040-30)
76420-040-607642000406060 TABLET, FILM COATED in 1 BOTTLE (76420-040-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c40d5c1d-9bd8-44aa-85a4-e1a34e1d3673

Use it

Look up 76420-040 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-040 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-040. 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.