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Cyclobenzaprine Hydrochloride

NDC 42708-172, Cyclobenzaprine Hydrochloride, tablet, film coated, from QPharma Inc.

Product NDC
42708-172
Status
Listed
Labeler
QPharma Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078643
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-172 \
  -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
42708-172-204270801722020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-172-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fbe6ba88-0581-50ef-e053-6394a90ab086

Use it

Look up 42708-172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-172. 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.