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LOFEXIDINE

NDC 85789-901, lofexidine hydrochloride, tablet, film coated, from BioCorRx Pharmaceuticals Inc.

Product NDC
85789-901
Status
Listed
Labeler
BioCorRx Pharmaceuticals Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA209229
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85789-901 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOFEXIDINE HYDROCHLORIDE.2 mg/1
Package NDCNDC-11Package
85789-901-368578909013636 TABLET, FILM COATED in 1 BOTTLE (85789-901-36)
85789-901-968578909019696 TABLET, FILM COATED in 1 BOTTLE (85789-901-96)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2dcc8288-adbe-45c3-b7bd-4d274001332d

Use it

Look up 85789-901 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85789-901 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85789-901. 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.