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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 52817-331, cyclobenzaprine hydrochloride, tablet, film coated, from TruPharma LLC.

Product NDC
52817-331
Status
Listed
Labeler
TruPharma LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208170
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52817-331 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE7.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
52817-331-1052817033110100 TABLET, FILM COATED in 1 BOTTLE (52817-331-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/08adc97f-feef-46fb-ac75-f015b4f3a43a

Use it

Look up 52817-331 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52817-331 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52817-331. 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.