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Lofexidine

NDC 71921-250, Lofexidine, tablet, coated, from Florida Pharmaceutical Products, LLC.

Product NDC
71921-250
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218613
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71921-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOFEXIDINE HYDROCHLORIDE.18 mg/1
Package NDCNDC-11Package
71921-250-36719210250361 BOTTLE in 1 CARTON (71921-250-36) / 36 TABLET, COATED in 1 BOTTLE
71921-250-96719210250961 BOTTLE in 1 CARTON (71921-250-96) / 96 TABLET, COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ce4488e2-842c-45ba-aca7-075a900e2a1c

  • NADAC price for package 71921025036

    GET /v1/drugs/nadac/71921025036

  • NADAC price for package 71921025096

    GET /v1/drugs/nadac/71921025096

Use it

Look up 71921-250 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71921-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71921-250. 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.