United States · FDA National Drug Code directory
Lofexidine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 14445-146_d60a5ecb-5e15-4ea7-bc53-a3740f00adff
- Product NDC
- 14445-146
- Form
- TABLET, COATED
- Composition / generic term
- Lofexidine
- Labeler
- Indoco Remedies Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240821
- Source listing expiry
- 20261231
Source-listed ingredients
- LOFEXIDINE HYDROCHLORIDE — .18 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (14445-146-36) / 36 TABLET, COATED in 1 BOTTLE · 14445-146-36
- 1 BOTTLE in 1 CARTON (14445-146-96) / 96 TABLET, COATED in 1 BOTTLE · 14445-146-96
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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