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Methocarbamol

NDC 85534-0022, methocarbamol, tablet, from HAWAII REPACK, INC..

Product NDC
85534-0022
Status
Listed
Labeler
HAWAII REPACK, 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/85534-0022 \
  -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
85534-0022-08553400220030 TABLET in 1 BOTTLE (85534-0022-0)
85534-0022-18553400220160 TABLET in 1 BOTTLE (85534-0022-1)
85534-0022-28553400220290 TABLET in 1 BOTTLE (85534-0022-2)
85534-0022-385534002203120 TABLET in 1 BOTTLE (85534-0022-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8643032a-c491-4ae4-ac46-5e0c4c79dc5b

Use it

Look up 85534-0022 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0022 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85534-0022. 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.