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
- 57237-322_86a71c33-cb93-4dac-9418-c3817ec65f76
- Product NDC
- 57237-322
- 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 — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 CARTON (57237-322-01) / 1 GUM, CHEWING in 1 BLISTER PACK · 57237-322-01
- 110 BLISTER PACK in 1 CARTON (57237-322-11) / 1 GUM, CHEWING in 1 BLISTER PACK · 57237-322-11
- 50 BLISTER PACK in 1 CARTON (57237-322-50) / 1 GUM, CHEWING in 1 BLISTER PACK · 57237-322-50
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.
Browse United States records →