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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 87441-010, cyclobenzaprine hydrochloride, tablet, film coated, from Unit Dose Solutions, Inc..

Product NDC
87441-010
Status
Listed
Labeler
Unit Dose Solutions, 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/87441-010 \
  -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
87441-010-018744100100130 TABLET, FILM COATED in 1 BLISTER PACK (87441-010-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/53bef1ab-55c0-cc52-e063-6394a90a12b3

Use it

Look up 87441-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87441-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87441-010. 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.