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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 85766-003, cyclobenzaprine hydrochloride, tablet, film coated, from Sportpharm LLC.

Product NDC
85766-003
Status
Listed
Labeler
Sportpharm LLC
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/85766-003 \
  -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
85766-003-00857660003001000 TABLET, FILM COATED in 1 BOTTLE (85766-003-00)
85766-003-01857660003011 TABLET, FILM COATED in 1 BOTTLE (85766-003-01)
85766-003-02857660003022 TABLET, FILM COATED in 1 BOTTLE (85766-003-02)
85766-003-04857660003044 TABLET, FILM COATED in 1 BOTTLE (85766-003-04)
85766-003-05857660003055 TABLET, FILM COATED in 1 BOTTLE (85766-003-05)
85766-003-07857660003077 TABLET, FILM COATED in 1 BOTTLE (85766-003-07)
85766-003-1085766000310100 TABLET, FILM COATED in 1 BOTTLE (85766-003-10)
85766-003-148576600031414 TABLET, FILM COATED in 1 BOTTLE (85766-003-14)
85766-003-208576600032020 TABLET, FILM COATED in 1 BOTTLE (85766-003-20)
85766-003-218576600032121 TABLET, FILM COATED in 1 BOTTLE (85766-003-21)
85766-003-308576600033030 TABLET, FILM COATED in 1 BOTTLE (85766-003-30)
85766-003-5085766000350500 TABLET, FILM COATED in 1 BOTTLE (85766-003-50)
85766-003-608576600036060 TABLET, FILM COATED in 1 BOTTLE (85766-003-60)
85766-003-908576600039090 TABLET, FILM COATED in 1 BOTTLE (85766-003-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d4e0f532-887b-40bb-80d6-5c4e5b1d64bf

Use it

Look up 85766-003 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85766-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85766-003. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.