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Lucemyra

NDC 78670-050, lofexidine hydrochloride, tablet, film coated, from USWM, LLC.

Product NDC
78670-050
Status
Listed
Labeler
USWM, LLC
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/78670-050 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOFEXIDINE HYDROCHLORIDE.2 mg/1
Package NDCNDC-11Package
78670-050-36786700050361 BOTTLE in 1 CARTON (78670-050-36) / 36 TABLET, FILM COATED in 1 BOTTLE
78670-050-96786700050961 BOTTLE in 1 CARTON (78670-050-96) / 96 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b748f308-ba71-4fd9-84ec-ec7e0f210885

  • NADAC price for package 78670005036

    GET /v1/drugs/nadac/78670005036

  • NADAC price for package 78670005096

    GET /v1/drugs/nadac/78670005096

Use it

Look up 78670-050 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/78670-050 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 78670-050. 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.