| 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 | |
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