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 |