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Methocarbamol

NDC 76420-667, methocarbamol, tablet, from Asclemed USA, Inc..

Product NDC
76420-667
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/76420-667 \
  -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
76420-667-0176420066701100 TABLET in 1 BOTTLE (76420-667-01)
76420-667-307642006673030 TABLET in 1 BOTTLE (76420-667-30)
76420-667-607642006676060 TABLET in 1 BOTTLE (76420-667-60)
76420-667-907642006679090 TABLET in 1 BOTTLE (76420-667-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1637e18d-d9f9-4171-99e6-4b866d821c87

Use it

Look up 76420-667 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-667 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-667. 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.