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Cyclobenzaprine Hydrochloride

NDC 71610-907, Cyclobenzaprine Hydrochloride, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-907
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077563
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-907 \
  -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
71610-907-457161009074545 TABLET, FILM COATED in 1 BOTTLE (71610-907-45)
71610-907-537161009075360 TABLET, FILM COATED in 1 BOTTLE (71610-907-53)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/34f4e63a-1259-0226-e063-6294a90a9fc4

Use it

Look up 71610-907 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-907 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-907. 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.