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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 85437-013, cyclobenzaprine hydrochloride, tablet, film coated, from Carol Way Pharma LLC.

Product NDC
85437-013
Status
Listed
Labeler
Carol Way Pharma 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/85437-013 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE7.5 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]

Package NDCNDC-11Package
85437-013-10854370013101000 TABLET, FILM COATED in 1 BOTTLE (85437-013-10)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5d0d6eec-28e8-6fca-e063-6294a90a59cd

Use it

Look up 85437-013 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85437-013 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85437-013. 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.