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Habitrol Patch
Habitrol Patch - 0067-4870-07 - (Nicotine)
Drug Information of Habitrol Patch
| Product NDC: | 0067-4870 |
| Proprietary Name: | Habitrol Patch |
| Non Proprietary Name: | Nicotine |
| Active Ingredient(s): | 21 mg/24h & nbsp; Nicotine |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Habitrol Patch
| Product NDC: | 0067-4870 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020076 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030226 |
Package Information of Habitrol Patch
| Package NDC: | 0067-4870-07 |
| Package Description: | 7 POUCH in 1 CARTON (0067-4870-07) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
NDC Information of Habitrol Patch
| NDC Code | 0067-4870-07 |
| Proprietary Name | Habitrol Patch |
| Package Description | 7 POUCH in 1 CARTON (0067-4870-07) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
| Product NDC | 0067-4870 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20030226 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | NICOTINE |
| Strength Number | 21 |
| Strength Unit | mg/24h |
| Pharmaceutical Classes |
