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Cyclobenzaprine Hydrochloride

NDC 69097-845, Cyclobenzaprine, tablet, film coated, from Cipla USA Inc..

Product NDC
69097-845
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090478
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-845 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69097-845-0769097084507100 TABLET, FILM COATED in 1 BOTTLE (69097-845-07)
69097-845-15690970845151000 TABLET, FILM COATED in 1 BOTTLE (69097-845-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/575a31fb-04c5-4001-88a7-c33adbacc6a8

  • NADAC price for package 69097084507

    GET /v1/drugs/nadac/69097084507

Use it

Look up 69097-845 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-845 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-845. 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.