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Methocarbamol

NDC 71335-0970, Methocarbamol, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-0970
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-0970 \
  -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
71335-0970-07133509700015 TABLET, FILM COATED in 1 BOTTLE (71335-0970-0)
71335-0970-17133509700114 TABLET, FILM COATED in 1 BOTTLE (71335-0970-1)
71335-0970-27133509700230 TABLET, FILM COATED in 1 BOTTLE (71335-0970-2)
71335-0970-37133509700320 TABLET, FILM COATED in 1 BOTTLE (71335-0970-3)
71335-0970-47133509700460 TABLET, FILM COATED in 1 BOTTLE (71335-0970-4)
71335-0970-571335097005100 TABLET, FILM COATED in 1 BOTTLE (71335-0970-5)
71335-0970-67133509700640 TABLET, FILM COATED in 1 BOTTLE (71335-0970-6)
71335-0970-77133509700790 TABLET, FILM COATED in 1 BOTTLE (71335-0970-7)
71335-0970-871335097008120 TABLET, FILM COATED in 1 BOTTLE (71335-0970-8)
71335-0970-9713350970097 TABLET, FILM COATED in 1 BOTTLE (71335-0970-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3212f121-9428-4186-8f00-accf08bca473

Use it

Look up 71335-0970 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0970 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0970. 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.