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Methocarbamol

NDC 85509-1770, Methocarbamol Tablets, tablet, coated, from PHOENIX RX LLC.

Product NDC
85509-1770
Status
Listed
Labeler
PHOENIX RX LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209312
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1770 \
  -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
85509-1770-38550917700330 TABLET, COATED in 1 BOTTLE (85509-1770-3)
85509-1770-68550917700660 TABLET, COATED in 1 BOTTLE (85509-1770-6)
85509-1770-98550917700990 TABLET, COATED in 1 BOTTLE (85509-1770-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/414b2fe0-fa2b-2b18-e063-6394a90ab2b9

Use it

Look up 85509-1770 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1770 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85509-1770. 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.