INATAL Ultra

Product NDC

63044-154

11-digit product format

630440154

Labeler code

63044

Product ID

63044-154_4b22195d-d683-4ced-ae90-2aa395765bf8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

INATAL Ultra

Dosage form

TABLET, COATED

Route

ORAL

Labeler

Nnodum Pharmaceuticals

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2005-06-20

Marketing end

0000-00-00

Substance

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 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

Pharmacologic 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

Current FDA listing

Historical FDA.report record