nicotine
Generic: nicotine polacrilex
Labeler: h e bDrug Facts
Product Profile
Brand Name
nicotine
Generic Name
nicotine polacrilex
Labeler
h e b
Dosage Form
GUM, CHEWING
Routes
Active Ingredients
nicotine 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37808-821
Product ID
37808-821_333acf23-416d-41c9-8d47-4f96a97df10d
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA079219
Listing Expiration
2026-12-31
Marketing Start
2022-10-28
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808821
Hyphenated Format
37808-821
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA079219 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 160 BLISTER PACK in 1 CARTON (37808-821-16) / 1 GUM, CHEWING in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "333acf23-416d-41c9-8d47-4f96a97df10d", "openfda": {"nui": ["N0000175706", "M0014836"], "unii": ["6M3C89ZY6R"], "rxcui": ["311975"], "spl_set_id": ["056ca637-d5b9-4790-a5a4-c9b58f93e88b"], "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 (37808-821-16) / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "37808-821-16", "marketing_start_date": "20221028"}], "brand_name": "Nicotine", "product_id": "37808-821_333acf23-416d-41c9-8d47-4f96a97df10d", "dosage_form": "GUM, CHEWING", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "37808-821", "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": "ANDA079219", "marketing_category": "ANDA", "marketing_start_date": "20221028", "listing_expiration_date": "20261231"}