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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 61919-261, CYCLOBENZAPRINE HYDROCHLORIDE, tablet, film coated, from Direct_Rx.

Product NDC
61919-261
Status
Listed
Labeler
Direct_Rx
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078722
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/61919-261 \
  -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
61919-261-156191902611515 TABLET, FILM COATED in 1 BOTTLE (61919-261-15)
61919-261-8261919026182180 TABLET, FILM COATED in 1 BOTTLE (61919-261-82)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels?ndc=61919-261

Use it

Look up 61919-261 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/61919-261 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 61919-261. 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.