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Lofexidine

NDC 70954-909, Lofexidine, tablet, from ANI Pharmaceuticals, Inc..

Product NDC
70954-909
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219917
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-909 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOFEXIDINE HYDROCHLORIDE.18 mg/1
Package NDCNDC-11Package
70954-909-107095409091036 TABLET in 1 BOTTLE (70954-909-10)
70954-909-207095409092096 TABLET in 1 BOTTLE (70954-909-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/335e26bf-b236-46d6-81cf-2879e5f3b1d9

  • NADAC price for package 70954090910

    GET /v1/drugs/nadac/70954090910

  • NADAC price for package 70954090920

    GET /v1/drugs/nadac/70954090920

Use it

Look up 70954-909 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-909 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-909. 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.