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Cyclobenzaprine Hydrochloride

NDC 70518-4174, Cyclobenzaprine Hydrochloride, capsule, extended release, from REMEDYREPACK INC..

Product NDC
70518-4174
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021777
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4174 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-4174-07051841740030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4174-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3175d24d-e8a0-4f14-bed9-a60ad59ac7e7

Use it

Look up 70518-4174 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4174 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4174. 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.