Product NDC: | 76439-221 |
Proprietary Name: | VP-ZEL |
Non Proprietary Name: | Niacinamide, Azelaic Acid, Zinc, Pyridoxine, Cupric Oxide, and Folic Acid |
Active Ingredient(s): | 5; 1.5; 500; 600; 5; 10 mg/1; mg/1; ug/1; mg/1; mg/1; mg/1 & nbsp; Niacinamide, Azelaic Acid, Zinc, Pyridoxine, Cupric Oxide, and Folic Acid |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76439-221 |
Labeler Name: | Virtus Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120301 |
Package NDC: | 76439-221-60 |
Package Description: | 60 TABLET, COATED in 1 BOTTLE (76439-221-60) |
NDC Code | 76439-221-60 |
Proprietary Name | VP-ZEL |
Package Description | 60 TABLET, COATED in 1 BOTTLE (76439-221-60) |
Product NDC | 76439-221 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Niacinamide, Azelaic Acid, Zinc, Pyridoxine, Cupric Oxide, and Folic Acid |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20120301 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Virtus Pharmaceuticals |
Substance Name | AZELAIC ACID; CUPRIC OXIDE; FOLIC ACID; NIACINAMIDE; PYRIDOXINE; ZINC |
Strength Number | 5; 1.5; 500; 600; 5; 10 |
Strength Unit | mg/1; mg/1; ug/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes | Decreased Protein Synthesis [PE],Decreased Sebaceous Gland Activity [PE] |