| Product NDC: | 75854-342 |
| Proprietary Name: | Nicomide |
| Non Proprietary Name: | niacinamide, folic acid, zinc oxide and cupric oxide |
| Active Ingredient(s): | 1.5; 500; 750; 25 mg/1; ug/1; mg/1; mg/1 & nbsp; niacinamide, folic acid, zinc oxide and cupric oxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75854-342 |
| Labeler Name: | Avion Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20121024 |
| Package NDC: | 75854-342-60 |
| Package Description: | 60 TABLET in 1 BOTTLE (75854-342-60) |
| NDC Code | 75854-342-60 |
| Proprietary Name | Nicomide |
| Package Description | 60 TABLET in 1 BOTTLE (75854-342-60) |
| Product NDC | 75854-342 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | niacinamide, folic acid, zinc oxide and cupric oxide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121024 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Avion Pharmaceuticals, LLC |
| Substance Name | CUPRIC OXIDE; FOLIC ACID; NIACINAMIDE; ZINC OXIDE |
| Strength Number | 1.5; 500; 750; 25 |
| Strength Unit | mg/1; ug/1; mg/1; mg/1 |
| Pharmaceutical Classes |