United States · FDA National Drug Code directory

Nicotine Polacrilex

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
57237-323_9230a5f3-bfa3-4a70-8e91-8df2736d9a29
Product NDC
57237-323
Form
GUM, CHEWING
Composition / generic term
Nicotine Polacrilex
Labeler
Rising Pharma Holdings, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20230810
Source listing expiry
20261231

Source-listed ingredients

  • NICOTINE — 4 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 BLISTER PACK in 1 CARTON (57237-323-01) / 1 GUM, CHEWING in 1 BLISTER PACK · 57237-323-01
  • 110 BLISTER PACK in 1 CARTON (57237-323-11) / 1 GUM, CHEWING in 1 BLISTER PACK · 57237-323-11
  • 50 BLISTER PACK in 1 CARTON (57237-323-50) / 1 GUM, CHEWING in 1 BLISTER PACK · 57237-323-50

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 Polacrilex — United States | Molindra Medicines