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Cyclobenzaprine Hydrochloride

NDC 68071-3805, Cyclobenzaprine Hydrochloride, tablet, film coated, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-3805
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208170
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3805 \
  -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
68071-3805-16807138050115 TABLET, FILM COATED in 1 BOTTLE (68071-3805-1)
68071-3805-26807138050220 TABLET, FILM COATED in 1 BOTTLE (68071-3805-2)
68071-3805-76807138050721 TABLET, FILM COATED in 1 BOTTLE (68071-3805-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2f89c8f6-7f3c-8396-e063-6294a90a643e

Use it

Look up 68071-3805 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3805 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3805. 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.