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Cyclobenzaprine Hydrochloride

NDC 65162-540, Cyclobenzaprine Hydrochloride, tablet, film coated, from Amneal Pharmaceuticals LLC.

Product NDC
65162-540
Status
Listed
Labeler
Amneal Pharmaceuticals 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/65162-540 \
  -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
65162-540-1065162054010100 TABLET, FILM COATED in 1 BOTTLE (65162-540-10)
65162-540-11651620540111000 TABLET, FILM COATED in 1 BOTTLE (65162-540-11)
65162-540-5065162054050500 TABLET, FILM COATED in 1 BOTTLE (65162-540-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/390151d4-5fcb-46e2-92e6-de184827f43d

Use it

Look up 65162-540 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-540 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-540. 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.