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NICOTINE TRANSDERMAL SYSTEM - 0067-5124-09 - (NICOTINE)

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Drug Information of NICOTINE TRANSDERMAL SYSTEM

Product NDC: 0067-5124
Proprietary Name: NICOTINE TRANSDERMAL SYSTEM
Non Proprietary Name: NICOTINE
Active Ingredient(s): 7    mg/24h & nbsp;   NICOTINE
Administration Route(s): TOPICAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of NICOTINE TRANSDERMAL SYSTEM

Product NDC: 0067-5124
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020076
Marketing Category: NDA
Start Marketing Date: 19991112

Package Information of NICOTINE TRANSDERMAL SYSTEM

Package NDC: 0067-5124-09
Package Description: 1 PATCH in 1 POUCH (0067-5124-09) > 24 h in 1 PATCH

NDC Information of NICOTINE TRANSDERMAL SYSTEM

NDC Code 0067-5124-09
Proprietary Name NICOTINE TRANSDERMAL SYSTEM
Package Description 1 PATCH in 1 POUCH (0067-5124-09) > 24 h in 1 PATCH
Product NDC 0067-5124
Product Type Name HUMAN OTC DRUG
Non Proprietary Name NICOTINE
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TOPICAL
Start Marketing Date 19991112
Marketing Category Name NDA
Labeler Name Novartis Consumer Health, Inc.
Substance Name NICOTINE
Strength Number 7
Strength Unit mg/24h
Pharmaceutical Classes

Complete Information of NICOTINE TRANSDERMAL SYSTEM


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