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Nicotine Polacrilex
Nicotine Polacrilex - 0172-6731-27 - (NICOTINE)
Drug Information of Nicotine Polacrilex
| Product NDC: | 0172-6731 |
| Proprietary Name: | Nicotine Polacrilex |
| Non Proprietary Name: | NICOTINE |
| Active Ingredient(s): | 4 mg/1 & nbsp; NICOTINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GUM, CHEWING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nicotine Polacrilex
| Product NDC: | 0172-6731 |
| Labeler Name: | IVAX Pharmaceuticals Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077850 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101115 |
Package Information of Nicotine Polacrilex
| Package NDC: | 0172-6731-27 |
| Package Description: | 108 BLISTER PACK in 1 BOX (0172-6731-27) > 1 GUM, CHEWING in 1 BLISTER PACK (0172-6731-00) |
NDC Information of Nicotine Polacrilex
| NDC Code | 0172-6731-27 |
| Proprietary Name | Nicotine Polacrilex |
| Package Description | 108 BLISTER PACK in 1 BOX (0172-6731-27) > 1 GUM, CHEWING in 1 BLISTER PACK (0172-6731-00) |
| Product NDC | 0172-6731 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | NICOTINE |
| Dosage Form Name | GUM, CHEWING |
| Route Name | ORAL |
| Start Marketing Date | 20101115 |
| Marketing Category Name | ANDA |
| Labeler Name | IVAX Pharmaceuticals Inc |
| Substance Name | NICOTINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
