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in control nicotine
in control nicotine - 37808-873-05 - (Nicotine Polacrilex)
Drug Information of in control nicotine
| Product NDC: | 37808-873 |
| 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): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of in control nicotine
| Product NDC: | 37808-873 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077007 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070725 |
Package Information of in control nicotine
| Package NDC: | 37808-873-05 |
| Package Description: | 3 VIAL in 1 CARTON (37808-873-05) > 24 LOZENGE in 1 VIAL |
NDC Information of in control nicotine
| NDC Code | 37808-873-05 |
| Proprietary Name | in control nicotine |
| Package Description | 3 VIAL in 1 CARTON (37808-873-05) > 24 LOZENGE in 1 VIAL |
| Product NDC | 37808-873 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20070725 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | NICOTINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
