mini nicotine
Generic: nicotine polacrilex
Labeler: atlantic biologicals corp.Drug Facts
Product Profile
Brand Name
mini nicotine
Generic Name
nicotine polacrilex
Labeler
atlantic biologicals corp.
Dosage Form
LOZENGE
Routes
Active Ingredients
nicotine 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
17856-1241
Product ID
17856-1241_3892fb10-9e99-9058-e063-6294a90a26b8
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA207868
Listing Expiration
2026-12-31
Marketing Start
2019-07-31
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
178561241
Hyphenated Format
17856-1241
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
mini nicotine (source: ndc)
Generic Name
nicotine polacrilex (source: ndc)
Application Number
ANDA207868 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 50 POUCH in 1 BOX (17856-1241-1) / 1 LOZENGE in 1 POUCH (17856-1241-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3892fb10-9e99-9058-e063-6294a90a26b8", "openfda": {"nui": ["N0000175706", "M0014836"], "unii": ["6M3C89ZY6R"], "rxcui": ["359818"], "spl_set_id": ["a0fc3eae-9c34-48af-bdd2-d95e91b68a9c"], "pharm_class_cs": ["Nicotine [CS]"], "pharm_class_epc": ["Cholinergic Nicotinic Agonist [EPC]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX (17856-1241-1) / 1 LOZENGE in 1 POUCH (17856-1241-2)", "package_ndc": "17856-1241-1", "marketing_start_date": "20240508"}], "brand_name": "Mini Nicotine", "product_id": "17856-1241_3892fb10-9e99-9058-e063-6294a90a26b8", "dosage_form": "LOZENGE", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "17856-1241", "generic_name": "Nicotine Polacrilex", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mini Nicotine", "active_ingredients": [{"name": "NICOTINE", "strength": "4 mg/1"}], "application_number": "ANDA207868", "marketing_category": "ANDA", "marketing_start_date": "20190731", "listing_expiration_date": "20261231"}