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Cyclobenzaprine hydrochloride

NDC 70518-4265, Cyclobenzaprine hydrochloride, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4265
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213324
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4265 \
  -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
70518-4265-07051842650090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4265-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/37056cab-953e-43ba-9b4c-163a739a52f7

Use it

Look up 70518-4265 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4265 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4265. 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.