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CYCLOBENZAPRINE HYDROCHLORIDE

NDC 11788-095, Cyclobenzaprine Hydrochloride, tablet, film coated, from AiPing Pharmaceutical, Inc..

Product NDC
11788-095
Status
Listed
Labeler
AiPing Pharmaceutical, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072854
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11788-095 \
  -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
11788-095-0111788009501100 TABLET, FILM COATED in 1 BOTTLE (11788-095-01)
11788-095-0511788009505500 TABLET, FILM COATED in 1 BOTTLE (11788-095-05)
11788-095-10117880095101000 TABLET, FILM COATED in 1 BOTTLE (11788-095-10)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 11788-095 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11788-095 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11788-095. 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.