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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 51655-539, cyclobenzaprine hydrochloride, tablet, film coated, from Northwind Health Company, LLC.

Product NDC
51655-539
Status
Listed
Labeler
Northwind Health Company, 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/51655-539 \
  -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
51655-539-205165505392020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-20)
51655-539-525165505395230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-52)
51655-539-535165505395310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-53)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dae3be94-a40c-5be1-e053-2a95a90a1484

Use it

Look up 51655-539 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-539 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-539. 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.