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Cyclobenzaprine Hydrochloride

NDC 70512-872, Cyclobenzaprine Hydrochloride, tablet, film coated, from SOLA Pharmaceuticals, LLC.

Product NDC
70512-872
Status
Listed
Labeler
SOLA Pharmaceuticals, 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/70512-872 \
  -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
70512-872-1070512087210100 TABLET, FILM COATED in 1 BOTTLE (70512-872-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/db930d05-3f92-41f1-888c-301b2c4565e6

  • NADAC price for package 70512087210

    GET /v1/drugs/nadac/70512087210

Use it

Look up 70512-872 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70512-872 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70512-872. 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.