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In Control Nicotine
In Control Nicotine - 37808-422-25 - (Nicotine Polacrilex)
Drug Information of In Control Nicotine
| Product NDC: | 37808-422 |
| Proprietary Name: | In Control Nicotine |
| Non Proprietary Name: | Nicotine Polacrilex |
| Active Ingredient(s): | 4 mg/1 & nbsp; Nicotine Polacrilex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GUM, CHEWING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of In Control Nicotine
| Product NDC: | 37808-422 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078326 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050615 |
Package Information of In Control Nicotine
| Package NDC: | 37808-422-25 |
| Package Description: | 11 BLISTER PACK in 1 CARTON (37808-422-25) > 10 GUM, CHEWING in 1 BLISTER PACK |
NDC Information of In Control Nicotine
| NDC Code | 37808-422-25 |
| Proprietary Name | In Control Nicotine |
| Package Description | 11 BLISTER PACK in 1 CARTON (37808-422-25) > 10 GUM, CHEWING in 1 BLISTER PACK |
| Product NDC | 37808-422 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | GUM, CHEWING |
| Route Name | ORAL |
| Start Marketing Date | 20050615 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | NICOTINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
