NDC 0135-0195

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 ID: 0135-0195_25db1674-fc71-4a47-91fa-be0e69542fca
• NDC: 0135-0195
• Product Type: Human Otc Drug
• Proprietary Name: NICODERM CQ
• Generic Name: Nicotine
• Dosage Form: Patch, Extended Release
• Route of Administration: TRANSDERMAL
• Marketing Start Date: 2011-05-12
• Marketing Category: NDA / NDA
• Application Number: NDA020165
• Labeler Name: GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• Substance Name: NICOTINE
• Active Ingredient Strength: 14 mg/24h
• Pharm Classes: Cholinergic Nicotinic Agonist [EPC], Nicotine [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0135-0195-02

14 PATCH in 1 CARTON (0135-0195-02) > 24 h in 1 PATCH

• Marketing Start Date: 2011-05-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0135-0195-02 [00135019502]

NICODERM CQ PATCH, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020165
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2011-05-12

NDC 0135-0195-08 [00135019508]

NICODERM CQ PATCH, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020165
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-05-12

NDC 0135-0195-03 [00135019503]

NICODERM CQ PATCH, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020165
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2011-05-12

NDC 0135-0195-05 [00135019505]

NICODERM CQ PATCH, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020165
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2011-05-12

Drug Details

Active Ingredients

Ingredient	Strength
NICOTINE	14 mg/24h

OpenFDA Data

• SPL SET ID: 93b2d1b9-83c1-40b5-b6af-90c38c8d6cef
• Manufacturer:
  • GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
• UNII:
  • 6M3C89ZY6R
• RxNorm Concept Unique ID - RxCUI:
  • 198029
  • 351429
  • 198031
  • 198030
  • 351427
  • 351433

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

NDC	Brand Name	Generic Name
0067-6011	Meijer NICOTINE TRANSDERMAL SYSTEM	NICOTINE
0067-6012	Meijer NICOTINE TRANSDERMAL SYSTEM	NICOTINE
0067-6013	Meijer NICOTINE TRANSDERMAL SYSTEM	NICOTINE
0135-0194	NICODERM	nicotine
0135-0195	NICODERM	nicotine
0135-0196	NICODERM	nicotine
0363-0451	Nicotine	Nicotine
0363-0455	Nicotine	Nicotine
0363-0457	Nicotine	Nicotine
0536-1106	NICOTINE	NICOTINE
0536-1107	NICOTINE	NICOTINE
0536-1108	NICOTINE	NICOTINE
0536-5894	Nicotine	Nicotine
0536-5895	Nicotine	Nicotine
0536-5896	Nicotine	Nicotine
11673-194	NICOTINE	nicotine
0220-3657	Nicotinum	NICOTINE
0009-5400	Nicotrol	nicotine
0009-5401	Nicotrol	nicotine