INATAL ADVANCE 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 Carbonate; Iron Pentacarbonyl; Cholecalciferol; Alpha-tocopherol Acetate; Thiamine Mononitrate; Riboflavin; Niacinamide; Pyridoxine Hydrochloride; Folic Acid; Cyanocobalamin; Zinc Oxide; Cupric Oxide; Magnesium Oxide; Docusate Sodium.
| Product ID | 63044-153_f48327a6-8aa3-41b4-bfa5-a1665174e5ef |
| NDC | 63044-153 |
| Product Type | Human Prescription Drug |
| Proprietary Name | INATAL ADVANCE |
| Generic Name | Inatal Advance |
| Dosage Form | Tablet, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2005-06-10 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Nnodum Pharmaceuticals |
| Substance Name | VITAMIN A; ASCORBIC ACID; CALCIUM CARBONATE; IRON PENTACARBONYL; CHOLECALCIFEROL; ALPHA-TOCOPHEROL ACETATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; ZINC OXIDE; CUPRIC OXIDE; MAGNESIUM 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; mg/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],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 | 2018-12-31 |
| Marketing Start Date | 2005-06-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-06-10 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-06-10 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| VITAMIN A | 2700 [iU]/1 |
| SPL SET ID: | 0674df74-3e12-4484-9ffd-3c73f982a727 |
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| UNII | |
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