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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 53746-540, CYCLOBENZAPRINE HYDROCHLORIDE, tablet, film coated, from Amneal Pharmaceuticals of New York LLC.

Product NDC
53746-540
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078218
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/53746-540 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
53746-540-0153746054001100 TABLET, FILM COATED in 1 BOTTLE (53746-540-01)
53746-540-0553746054005500 TABLET, FILM COATED in 1 BOTTLE (53746-540-05)
53746-540-10537460540101000 TABLET, FILM COATED in 1 BOTTLE (53746-540-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/31bb92f6-ec8c-4636-8b07-8814417fe78e

Use it

Look up 53746-540 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53746-540 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53746-540. 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.