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Nicotine
Nicotine - 0536-5896-88 - (Nicotine)
Drug Information of Nicotine
| Product NDC: | 0536-5896 |
| Proprietary Name: | Nicotine |
| Non Proprietary Name: | Nicotine |
| Active Ingredient(s): | 21 mg/24h & nbsp; Nicotine |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nicotine
| Product NDC: | 0536-5896 |
| Labeler Name: | Rugby Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074612 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19971020 |
Package Information of Nicotine
| Package NDC: | 0536-5896-88 |
| Package Description: | 14 POUCH in 1 CARTON (0536-5896-88) > 1 PATCH in 1 POUCH (0536-5896-33) > 24 h in 1 PATCH |
NDC Information of Nicotine
| NDC Code | 0536-5896-88 |
| Proprietary Name | Nicotine |
| Package Description | 14 POUCH in 1 CARTON (0536-5896-88) > 1 PATCH in 1 POUCH (0536-5896-33) > 24 h in 1 PATCH |
| Product NDC | 0536-5896 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine |
| Dosage Form Name | PATCH |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 19971020 |
| Marketing Category Name | ANDA |
| Labeler Name | Rugby Laboratories, Inc. |
| Substance Name | NICOTINE |
| Strength Number | 21 |
| Strength Unit | mg/24h |
| Pharmaceutical Classes |
