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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 80425-0498, cyclobenzaprine hydrochloride, tablet, film coated, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0498
Status
Listed
Labeler
Advanced Rx of Tennessee, 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/80425-0498 \
  -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
80425-0498-18042504980130 TABLET, FILM COATED in 1 BOTTLE (80425-0498-1)
80425-0498-28042504980260 TABLET, FILM COATED in 1 BOTTLE (80425-0498-2)
80425-0498-38042504980390 TABLET, FILM COATED in 1 BOTTLE (80425-0498-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/30ca08c7-4ee3-2f37-e063-6294a90ae31a

Use it

Look up 80425-0498 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0498 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0498. 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.