INATAL Ultra is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Nnodum Pharmaceuticals. The primary component is Vitamin A; Ascorbic Acid; Calcium Citrate; Iron Pentacarbonyl; Cholecalciferol; Alpha-tocopherol Acetate; Thiamine Mononitrate; Riboflavin; Niacinamide; Pyridoxine Hydrochloride; Folic Acid; Cyanocobalamin; Potassium Iodide; Zinc Oxide; Cupric Oxide; Docusate Sodium.
| Product ID | 63044-154_4b22195d-d683-4ced-ae90-2aa395765bf8 |
| NDC | 63044-154 |
| Product Type | Human Prescription Drug |
| Proprietary Name | INATAL Ultra |
| Generic Name | Inatal Ultra |
| Dosage Form | Tablet, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2005-06-20 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Nnodum Pharmaceuticals |
| Substance Name | VITAMIN A; ASCORBIC ACID; CALCIUM CITRATE; IRON PENTACARBONYL; CHOLECALCIFEROL; ALPHA-TOCOPHEROL ACETATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; POTASSIUM IODIDE; ZINC OXIDE; CUPRIC OXIDE; DOCUSATE SODIUM |
| Active Ingredient Strength | 2700 [iU]/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1 |
| Pharm Classes | Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Calcium [CS],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],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],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2005-06-20 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-06-20 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-06-20 |
| Inactivation Date | 2019-10-21 |
| Ingredient | Strength |
|---|---|
| VITAMIN A | 2700 [iU]/1 |
| SPL SET ID: | 864fdaeb-a030-4ebd-93f1-a51d4e8eaa94 |
| Manufacturer | |
| UNII |