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Nicorelief
Nicorelief - 0904-5736-51 - (Nicotine Polacrilex)
Drug Information of Nicorelief
| Product NDC: | 0904-5736 |
| Proprietary Name: | Nicorelief |
| 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 Nicorelief
| Product NDC: | 0904-5736 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078325 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050412 |
Package Information of Nicorelief
| Package NDC: | 0904-5736-51 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (0904-5736-51) > 10 GUM, CHEWING in 1 BLISTER PACK |
NDC Information of Nicorelief
| NDC Code | 0904-5736-51 |
| Proprietary Name | Nicorelief |
| Package Description | 5 BLISTER PACK in 1 CARTON (0904-5736-51) > 10 GUM, CHEWING in 1 BLISTER PACK |
| Product NDC | 0904-5736 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | GUM, CHEWING |
| Route Name | ORAL |
| Start Marketing Date | 20050412 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | NICOTINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
