Product NDC: | 50967-317 |
Proprietary Name: | NESTABS DHA |
Non Proprietary Name: | Sodium Ascorbate, Cholecalciferol, di-alpha-Tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine HCL, Folic Acid, Cyanocobalamin, Calcium Formate, Calcium Carbonate, Ferrous ( |
Active Ingredient(s): | & nbsp; Sodium Ascorbate, Cholecalciferol, di-alpha-Tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine HCL, Folic Acid, Cyanocobalamin, Calcium Formate, Calcium Carbonate, Ferrous ( |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50967-317 |
Labeler Name: | WOMENS CHOICE PHARMACEUTICALS LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110201 |
Package NDC: | 50967-317-30 |
Package Description: | 4 BLISTER PACK in 1 CARTON (50967-317-30) > 1 KIT in 1 BLISTER PACK |
NDC Code | 50967-317-30 |
Proprietary Name | NESTABS DHA |
Package Description | 4 BLISTER PACK in 1 CARTON (50967-317-30) > 1 KIT in 1 BLISTER PACK |
Product NDC | 50967-317 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Ascorbate, Cholecalciferol, di-alpha-Tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine HCL, Folic Acid, Cyanocobalamin, Calcium Formate, Calcium Carbonate, Ferrous ( |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20110201 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | WOMENS CHOICE PHARMACEUTICALS LLC |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |