nicotine transdermal

Generic: nicotine

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name nicotine transdermal
Generic Name nicotine
Labeler rite aid corporation
Dosage Form KIT
Routes
TRANSDERMAL
Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-3627
Product ID 11822-3627_cc8505c5-38ba-5bb3-5c4d-0e7a1984eae4
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA020076
Listing Expiration 2026-12-31
Marketing Start 2021-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118223627
Hyphenated Format 11822-3627

Supplemental Identifiers

RxCUI
198029 198030 198031 892244

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 transdermal (source: ndc)
Generic Name nicotine (source: ndc)
Application Number NDA020076 (source: ndc)
Routes
TRANSDERMAL
source: ndc

Resolved Composition

Strengths
  • 21 mg
  • 14 mg
  • 7 mg
source: label
Packaging
  • 56 PATCH in 1 CARTON (11822-3627-3) / 1 KIT in 1 PATCH
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TRANSDERMAL"], "spl_id": "cc8505c5-38ba-5bb3-5c4d-0e7a1984eae4", "openfda": {"rxcui": ["198029", "198030", "198031", "892244"], "spl_set_id": ["ae6027da-5c96-ed47-e1ae-e900fc0f72ce"], "manufacturer_name": ["Rite Aid Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "56 PATCH in 1 CARTON (11822-3627-3)  / 1 KIT in 1 PATCH", "package_ndc": "11822-3627-3", "marketing_start_date": "20210331"}], "brand_name": "NICOTINE TRANSDERMAL", "product_id": "11822-3627_cc8505c5-38ba-5bb3-5c4d-0e7a1984eae4", "dosage_form": "KIT", "product_ndc": "11822-3627", "generic_name": "NICOTINE", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NICOTINE", "brand_name_suffix": "TRANSDERMAL", "application_number": "NDA020076", "marketing_category": "NDA", "marketing_start_date": "20210331", "listing_expiration_date": "20261231"}