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Cyclobenzaprine Hydrochloride

NDC 69420-1001, Cyclobenzaprine Hydrochloride, tablet, film coated, from SA3, LLC.

Product NDC
69420-1001
Status
Listed
Labeler
SA3, LLC
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/69420-1001 \
  -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
69420-1001-1694201001011000 TABLET, FILM COATED in 1 BOTTLE (69420-1001-1)
69420-1001-269420100102100 TABLET, FILM COATED in 1 BOTTLE (69420-1001-2)
69420-1001-36942010010330 TABLET, FILM COATED in 1 BOTTLE (69420-1001-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a4ae481f-9e47-470a-b4d1-5a33c0df8761

Use it

Look up 69420-1001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69420-1001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69420-1001. 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.