nicotine

Generic: nicotine polacrilex

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nicotine
Generic Name nicotine polacrilex
Labeler h e b
Dosage Form GUM, CHEWING
Routes
ORAL
Active Ingredients

nicotine 4 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-658
Product ID 37808-658_71077dd2-ec82-4e1a-b8fd-7a6c65628814
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076779
Listing Expiration 2026-12-31
Marketing Start 2019-05-03

Pharmacologic Class

Established (EPC)
cholinergic nicotinic agonist [epc]
Chemical Structure
nicotine [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808658
Hyphenated Format 37808-658

Supplemental Identifiers

RxCUI
311975
UNII
6M3C89ZY6R
NUI
N0000175706 M0014836

Packaging Origin

Original Packager
true

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 nicotine (source: ndc)
Generic Name nicotine polacrilex (source: ndc)
Application Number ANDA076779 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 160 BLISTER PACK in 1 CARTON (37808-658-06) / 1 GUM, CHEWING in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

nicotine (4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "71077dd2-ec82-4e1a-b8fd-7a6c65628814", "openfda": {"nui": ["N0000175706", "M0014836"], "unii": ["6M3C89ZY6R"], "rxcui": ["311975"], "spl_set_id": ["c690001d-12c4-4a0f-b9b0-2d2b73dcd93a"], "pharm_class_cs": ["Nicotine [CS]"], "pharm_class_epc": ["Cholinergic Nicotinic Agonist [EPC]"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "160 BLISTER PACK in 1 CARTON (37808-658-06)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "37808-658-06", "marketing_start_date": "20190503"}], "brand_name": "Nicotine", "product_id": "37808-658_71077dd2-ec82-4e1a-b8fd-7a6c65628814", "dosage_form": "GUM, CHEWING", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "37808-658", "generic_name": "nicotine polacrilex", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nicotine", "active_ingredients": [{"name": "NICOTINE", "strength": "4 mg/1"}], "application_number": "ANDA076779", "marketing_category": "ANDA", "marketing_start_date": "20190503", "listing_expiration_date": "20261231"}