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Cyclobenzaprine Hydrochloride

NDC 50268-190, Cyclobenzaprine Hydrochloride, tablet, film coated, from AvPAK.

Product NDC
50268-190
Status
Listed
Labeler
AvPAK
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090478
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-190 \
  -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
50268-190-155026801901550 BLISTER PACK in 1 BOX (50268-190-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-190-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/64f6d1be-4067-a5c7-2343-4aed651a0cac

  • NADAC price for package 50268019015

    GET /v1/drugs/nadac/50268019015

Use it

Look up 50268-190 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-190 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-190. 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.