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Cyclobenzaprine hydrochloride

NDC 29300-414, Cyclobenzaprine hydrochloride, tablet, film coated, from Unichem Pharmaceuticals (USA), Inc..

Product NDC
29300-414
Status
Listed
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213324
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/29300-414 \
  -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
29300-414-0129300041401100 TABLET, FILM COATED in 1 BOTTLE (29300-414-01)
29300-414-10293000414101000 TABLET, FILM COATED in 1 BOTTLE (29300-414-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1adcdd8a-30f9-4a7b-853c-948a5589acab

  • NADAC price for package 29300041401

    GET /v1/drugs/nadac/29300041401

Use it

Look up 29300-414 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/29300-414 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 29300-414. 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.