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CHLORZOXAZONE

NDC 71205-711, CHLORZOXAZONE, tablet, from Proficient Rx LP.

Product NDC
71205-711
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA089853
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-711 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORZOXAZONE500 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]

Package NDCNDC-11Package
71205-711-207120507112020 TABLET in 1 BOTTLE (71205-711-20)
71205-711-307120507113030 TABLET in 1 BOTTLE (71205-711-30)
71205-711-607120507116060 TABLET in 1 BOTTLE (71205-711-60)
71205-711-907120507119090 TABLET in 1 BOTTLE (71205-711-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0a8ee5fa-f393-4568-81bd-269f9a4cecd6

Use it

Look up 71205-711 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-711 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-711. 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.