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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 85534-0085, cyclobenzaprine hydrochloride, tablet, film coated, from HAWAII REPACK, INC..

Product NDC
85534-0085
Status
Listed
Labeler
HAWAII REPACK, 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/85534-0085 \
  -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
85534-0085-08553400850030 TABLET, FILM COATED in 1 BOTTLE (85534-0085-0)
85534-0085-18553400850160 TABLET, FILM COATED in 1 BOTTLE (85534-0085-1)
85534-0085-28553400850290 TABLET, FILM COATED in 1 BOTTLE (85534-0085-2)
85534-0085-385534008503120 TABLET, FILM COATED in 1 BOTTLE (85534-0085-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cf5d4de9-79c3-4935-be69-89e98d7b54cc

Use it

Look up 85534-0085 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0085 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85534-0085. 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.