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sunmark nicotine
sunmark nicotine - 49348-573-08 - (Nicotine Polacrilex)
Drug Information of sunmark nicotine
| Product NDC: | 49348-573 |
| 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): | GUM, CHEWING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark nicotine
| Product NDC: | 49348-573 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076775 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050618 |
Package Information of sunmark nicotine
| Package NDC: | 49348-573-08 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (49348-573-08) > 10 GUM, CHEWING in 1 BLISTER PACK |
NDC Information of sunmark nicotine
| NDC Code | 49348-573-08 |
| Proprietary Name | sunmark nicotine |
| Package Description | 5 BLISTER PACK in 1 CARTON (49348-573-08) > 10 GUM, CHEWING in 1 BLISTER PACK |
| Product NDC | 49348-573 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Nicotine Polacrilex |
| Dosage Form Name | GUM, CHEWING |
| Route Name | ORAL |
| Start Marketing Date | 20050618 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | NICOTINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
