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zonnic nicotine polacrilex
zonnic nicotine polacrilex - 42884-456-52 - (Nicotine Polacrilex)
Drug Information of zonnic nicotine polacrilex
| Product NDC: | 42884-456 |
| Proprietary Name: | zonnic nicotine polacrilex |
| Non Proprietary Name: | Nicotine Polacrilex |
| Active Ingredient(s): | 2 mg/1 & nbsp; Nicotine Polacrilex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GUM, CHEWING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of zonnic nicotine polacrilex
| Product NDC: | 42884-456 |
| Labeler Name: | Niconovum USA Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076777 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120625 |
Package Information of zonnic nicotine polacrilex
| Package NDC: | 42884-456-52 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (42884-456-52) > 10 GUM, CHEWING in 1 BLISTER PACK |
NDC Information of zonnic nicotine polacrilex
| NDC Code | 42884-456-52 |
| Proprietary Name | zonnic nicotine polacrilex |
| Package Description | 1 BLISTER PACK in 1 CARTON (42884-456-52) > 10 GUM, CHEWING in 1 BLISTER PACK |
| Product NDC | 42884-456 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | GUM, CHEWING |
| Route Name | ORAL |
| Start Marketing Date | 20120625 |
| Marketing Category Name | ANDA |
| Labeler Name | Niconovum USA Inc. |
| Substance Name | NICOTINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
