| NDC Code: |
59088-114 |
| Proprietary Name: |
PureFe Plus |
| Suffix: |
|
| Non-Proprietary Name: |
Ferrous Fumarate |
| Dosage Form: |
CAPSULE |
| Method: |
ORAL |
| Original Marketing Date: |
01-06-2011 |
| Category Name: |
UNAPPROVED DRUG OTHER |
| Application Number: |
|
| Labeler: |
PURETEK CORPORATION |
| Substance Name: |
CALCIUM PANTOTHENATE; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM SULFATE, UNSPECIFIED; MANGANESE SULFATE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE |
| Active Numerator Strength: |
10; .8; 15; 106; 1; 6.9; 1.3; 30; 5; 6; 200; 10; 18.2 |
| Active Ingredient Unit: |
mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 |
| Pharm Classes: |
Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE] |
| DEA Schedule: |
|
