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INATAL Ultra - INATAL Ultra

Navigation: NDC > Supplier starting with: N > NNODUM PHARMACEUTICALS
Field Value
NDC Code: 63044-154
Proprietary Name: INATAL Ultra
Suffix:
Non-Proprietary Name: INATAL Ultra
Dosage Form: TABLET, COATED
Method: ORAL
Original Marketing Date: 20-06-2005
Category Name: UNAPPROVED DRUG OTHER
Application Number:
Labeler: NNODUM PHARMACEUTICALS
Substance Name: ALPHA-TOCOPHEROL ACETATE; ASCORBIC ACID; CALCIUM CITRATE; CHOLECALCIFEROL; CUPRIC OXIDE; CYANOCOBALAMIN; DOCUSATE SODIUM; FOLIC ACID; IRON PENTACARBONYL; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; VITAMIN A; ZINC OXIDE
Active Numerator Strength: 30; 120; 200; 400; 2; 12; 50; 1; 90; 20; 150; 20; 3.4; 3; 2700; 25
Active Ingredient Unit: [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; [iU]/1; mg/1
Pharm Classes: Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]
DEA Schedule: