United States · FDA National Drug Code directory

Nicotine Transdermal System

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
50742-669_5244921a-4ef6-b582-e063-6294a90a8845
Product NDC
50742-669
Form
PATCH
Composition / generic term
Nicotine Transdermal System
Labeler
Ingenus Pharmaceuticals, LLC
Marketing category
ANDA
Marketing start / end (source format)
20260519
Source listing expiry
20271231

Source-listed ingredients

  • NICOTINE — 14 mg/24h

These values do not establish equivalence or a dose recommendation.

Packages

  • 7 POUCH in 1 CARTON (50742-669-07) / 24 h in 1 POUCH · 50742-669-07
  • 14 POUCH in 1 CARTON (50742-669-14) / 24 h in 1 POUCH · 50742-669-14
  • 28 POUCH in 1 CARTON (50742-669-28) / 24 h in 1 POUCH · 50742-669-28

Source and coverage

Open FDA National Drug Code directory

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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Nicotine Transdermal System — United States | Molindra Medicines