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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 42708-197, cyclobenzaprine hydrochloride, tablet, film coated, from QPharma, Inc..

Product NDC
42708-197
Status
Listed
Labeler
QPharma, Inc.
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/42708-197 \
  -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
42708-197-204270801972020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-197-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4dcbdf8f-37ce-0f90-e063-6394a90ae83c

Use it

Look up 42708-197 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-197 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-197. 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.