Habitrol Step 2 is a Transdermal Patch, Extended Release in the Human Otc Drug category. It is labeled and distributed by Dr. Reddy's Laboratories Inc.. The primary component is Nicotine.
| Product ID | 55741-447_dab0788a-60c8-316c-7c69-cda848fb1fe7 |
| NDC | 55741-447 |
| Product Type | Human Otc Drug |
| Proprietary Name | Habitrol Step 2 |
| Generic Name | Nicotine Transdermal System Patch |
| Dosage Form | Patch, Extended Release |
| Route of Administration | TRANSDERMAL |
| Marketing Start Date | 2018-07-13 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020076 |
| Labeler Name | Dr. Reddy's Laboratories Inc. |
| Substance Name | NICOTINE |
| Active Ingredient Strength | 14 mg/24h |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-07-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA020076 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-04-22 |
| Marketing Category | NDA |
| Application Number | NDA020076 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-07-01 |
| Ingredient | Strength |
|---|---|
| NICOTINE | 14 mg/24h |
| SPL SET ID: | 051be7ae-6504-c2d8-7424-2e328e4fcfc2 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 55741-446 | Habitrol | Nicotine Transdermal System Patch |
| 55741-447 | Habitrol | Nicotine Transdermal System Patch |
| 55741-448 | Habitrol | Nicotine Transdermal System Patch |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HABITROL 86322221 4637378 Live/Registered |
NOVARTIS AG 2014-06-27 |
![]() HABITROL 75677145 2825365 Dead/Cancelled |
Novartis AG 1999-04-08 |
![]() HABITROL 74088810 1757530 Dead/Cancelled |
NOVARTIS CONSUMER HEALTH, INC. 1990-08-17 |