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Cyclobenzaprine Hydrochloride

NDC 70518-4692, Cyclobenzaprine Hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-4692
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218936
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4692 \
  -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
70518-4692-07051846920030 TABLET in 1 BOTTLE, PLASTIC (70518-4692-0)
70518-4692-17051846920112 TABLET in 1 BOTTLE, PLASTIC (70518-4692-1)
70518-4692-2705184692025 TABLET in 1 BOTTLE, PLASTIC (70518-4692-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/34e57aff-dc4b-4631-9d57-31020244835d

Use it

Look up 70518-4692 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4692 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4692. 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.