NDC 0135-0194

NICODERM CQ

Nicotine

NICODERM CQ is a Transdermal Patch, Extended Release in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Nicotine.

Product ID0135-0194_25db1674-fc71-4a47-91fa-be0e69542fca
NDC0135-0194
Product TypeHuman Otc Drug
Proprietary NameNICODERM CQ
Generic NameNicotine
Dosage FormPatch, Extended Release
Route of AdministrationTRANSDERMAL
Marketing Start Date2011-05-12
Marketing CategoryNDA / NDA
Application NumberNDA020165
Labeler NameGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameNICOTINE
Active Ingredient Strength21 mg/24h
Pharm ClassesCholinergic Nicotinic Agonist [EPC], Nicotine [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0135-0194-01

7 PATCH in 1 CARTON (0135-0194-01) > 24 h in 1 PATCH
Marketing Start Date2011-05-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0135-0194-05 [00135019405]

NICODERM CQ PATCH, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020165
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-05-12

NDC 0135-0194-08 [00135019408]

NICODERM CQ PATCH, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020165
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-12

NDC 0135-0194-01 [00135019401]

NICODERM CQ PATCH, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020165
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-05-12

NDC 0135-0194-02 [00135019402]

NICODERM CQ PATCH, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020165
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-05-12

NDC 0135-0194-03 [00135019403]

NICODERM CQ PATCH, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020165
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-05-12

Drug Details

Active Ingredients

IngredientStrength
NICOTINE21 mg/24h

OpenFDA Data

SPL SET ID:93b2d1b9-83c1-40b5-b6af-90c38c8d6cef
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198029
  • 351429
  • 198031
  • 198030
  • 351427
  • 351433

    • NDC Crossover Matching brand name "NICODERM CQ" or generic name "Nicotine"

    NDCBrand NameGeneric Name
    0067-6011Meijer NICOTINE TRANSDERMAL SYSTEMNICOTINE
    0067-6012Meijer NICOTINE TRANSDERMAL SYSTEMNICOTINE
    0067-6013Meijer NICOTINE TRANSDERMAL SYSTEMNICOTINE
    0135-0194NICODERMnicotine
    0135-0195NICODERMnicotine
    0135-0196NICODERMnicotine
    0363-0451NicotineNicotine
    0363-0455NicotineNicotine
    0363-0457NicotineNicotine
    0536-1106NICOTINENICOTINE
    0536-1107NICOTINENICOTINE
    0536-1108NICOTINENICOTINE
    0536-5894NicotineNicotine
    0536-5895NicotineNicotine
    0536-5896NicotineNicotine
    11673-194NICOTINEnicotine
    0220-3657NicotinumNICOTINE
    0009-5400Nicotrolnicotine
    0009-5401Nicotrolnicotine

    Trademark Results [NICODERM]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    NICODERM
    NICODERM
    75411022 2222726 Live/Registered
    AVENTISUB LLC
    1997-12-20
    NICODERM
    NICODERM
    73806916 1577275 Live/Registered
    MERRELL DOW PHARMACEUTICALS INC.
    1989-06-15
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