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Cyclobenzaprine Hydrochloride

NDC 59746-211, Cyclobenzaprine Hydrochloride, tablet, film coated, from Jubilant Cadista Pharmaceuticals Inc..

Product NDC
59746-211
Status
Listed
Labeler
Jubilant Cadista Pharmaceuticals Inc.
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/59746-211 \
  -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
59746-211-0659746021106100 TABLET, FILM COATED in 1 BOTTLE (59746-211-06)
59746-211-10597460211101000 TABLET, FILM COATED in 1 BOTTLE (59746-211-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/592871f6-0eb2-4624-9e10-bd8bf767c002

Use it

Look up 59746-211 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59746-211 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59746-211. 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.