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Cyclobenzaprine Hydrochloride

NDC 72162-1359, cyclobenzaprine hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
72162-1359
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077797
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1359 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72162-1359-0721621359001000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-0)
72162-1359-172162135901100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-1)
72162-1359-572162135905500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/90c7a982-6442-4241-a60b-b5dfab2abb71

Use it

Look up 72162-1359 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1359 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1359. 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.