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Cyclobenzaprine Hydrochloride

NDC 68071-2790, Cyclobenzaprine Hydrochloride, tablet, film coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2790
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078643
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2790 \
  -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
68071-2790-16807127900110 TABLET, FILM COATED in 1 BOTTLE (68071-2790-1)
68071-2790-26807127900212 TABLET, FILM COATED in 1 BOTTLE (68071-2790-2)
68071-2790-66807127900660 TABLET, FILM COATED in 1 BOTTLE (68071-2790-6)
68071-2790-76807127900720 TABLET, FILM COATED in 1 BOTTLE (68071-2790-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e3b5fc92-9186-6944-e053-2a95a90a1c9f

Use it

Look up 68071-2790 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2790 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2790. 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.