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Sunmark Nicotine
Sunmark Nicotine - 49348-852-16 - (Nicotine Polacrilex)
Drug Information of Sunmark Nicotine
| Product NDC: | 49348-852 |
| Proprietary Name: | Sunmark Nicotine |
| Non Proprietary Name: | Nicotine Polacrilex |
| Active Ingredient(s): | 2 mg/1 & nbsp; Nicotine Polacrilex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark Nicotine
| Product NDC: | 49348-852 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077007 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080507 |
Package Information of Sunmark Nicotine
| Package NDC: | 49348-852-16 |
| Package Description: | 3 VIAL in 1 CARTON (49348-852-16) > 24 LOZENGE in 1 VIAL |
NDC Information of Sunmark Nicotine
| NDC Code | 49348-852-16 |
| Proprietary Name | Sunmark Nicotine |
| Package Description | 3 VIAL in 1 CARTON (49348-852-16) > 24 LOZENGE in 1 VIAL |
| Product NDC | 49348-852 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20080507 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | NICOTINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
