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Lofexidine hydrochloride

NDC 66993-345, lofexidine hydrochloride, tablet, film coated, from Prasco Laboratories.

Product NDC
66993-345
Status
Listed
Labeler
Prasco Laboratories
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA209229
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/66993-345 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOFEXIDINE HYDROCHLORIDE.2 mg/1
Package NDCNDC-11Package
66993-345-37669930345371 BOTTLE in 1 CARTON (66993-345-37) / 36 TABLET, FILM COATED in 1 BOTTLE
66993-345-76669930345761 BOTTLE in 1 CARTON (66993-345-76) / 96 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/77367dfa-434f-4d61-95fe-f0f1628457d1

  • NADAC price for package 66993034537

    GET /v1/drugs/nadac/66993034537

  • NADAC price for package 66993034576

    GET /v1/drugs/nadac/66993034576

Use it

Look up 66993-345 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66993-345 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66993-345. 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.