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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 85509-1014, cyclobenzaprine hydrochloride, tablet, film coated, from PHOENIX RX LLC.

Product NDC
85509-1014
Status
Listed
Labeler
PHOENIX RX 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/85509-1014 \
  -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
85509-1014-38550910140330 TABLET, FILM COATED in 1 BOTTLE (85509-1014-3)
85509-1014-68550910140660 TABLET, FILM COATED in 1 BOTTLE (85509-1014-6)
85509-1014-98550910140990 TABLET, FILM COATED in 1 BOTTLE (85509-1014-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3a90171b-aef3-0691-e063-6294a90a6560

Use it

Look up 85509-1014 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1014 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85509-1014. 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.