NESTABS Prenatal Multi-vitamin/Mineral Supplement is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Womens Choice Pharmaceuticals Llc. The primary component is Sodium Ascorbate; Cholecalciferol; .alpha.-tocopherol Acetate, D-; Thiamine Mononitrate; Riboflavin; Niacinamide; Pyridoxine Hydrochloride; Folic Acid; Cyanocobalamin; Calcium Formate; Calcium Carbonate; Ferrous Bisglycinate; Potassium Iodide; Zinc Oxide; Choline Bitartrate.
Product ID | 50967-219_63d82922-1e02-47f5-a64e-e97e2e1ba4ad |
NDC | 50967-219 |
Product Type | Human Prescription Drug |
Proprietary Name | NESTABS Prenatal Multi-vitamin/Mineral Supplement |
Generic Name | Multi-vitamin/mineral Supplement With Sodium Ascorbate, Cholecalciferol, Di-alpha-tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hcl, Folic Acid, Cyanocobalamin, Calcium |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2011-02-01 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | WOMENS CHOICE PHARMACEUTICALS LLC |
Substance Name | SODIUM ASCORBATE; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE, D-; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM FORMATE; CALCIUM CARBONATE; FERROUS BISGLYCINATE; POTASSIUM IODIDE; ZINC OXIDE; CHOLINE BITARTRATE |
Active Ingredient Strength | 120 mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1 |
Pharm Classes | Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Calcium [CS],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2011-02-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-02-01 |
Ingredient | Strength |
---|---|
SODIUM ASCORBATE | 120 mg/1 |
SPL SET ID: | 61945c85-3c9a-4b57-a8e1-79dd0469a042 |
Manufacturer | |
UNII | |
UPC Code |
Mark Image Registration | Serial | Company Trademark Application Date |
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![]() NESTABS 72097201 0712037 Dead/Cancelled |
Georges, George P. 1960-05-16 |