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NDC 59088-0112-66 PureVit DualFe Plus 10; .8; 15; 53; 1; 53; 1.3; 30; 5; 6; 200; 10; 18.2 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 Details
PureVit DualFe Plus 10; .8; 15; 53; 1; 53; 1.3; 30; 5; 6; 200; 10; 18.2 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
PureVit DualFe Plus is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is CALCIUM PANTOTHENATE; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; IRON DEXTRAN; MANGANESE SULFATE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE.
Product Information
| NDC | 59088-0112 |
|---|---|
| Product ID | 59088-112_f2048b24-433b-98ba-e053-2995a90a5e85 |
| Associated GPIs | 82992008600130 |
| GCN Sequence Number | 060711 |
| GCN Sequence Number Description | iron fm,ps no.1/folic/mv no.18 CAPSULE 106 MG-1MG ORAL |
| HIC3 | C3B |
| HIC3 Description | IRON REPLACEMENT |
| GCN | 26937 |
| HICL Sequence Number | 033611 |
| HICL Sequence Number Description | IRON FUMARATE-IRON POLYSACCH CPLEX/FOLIC ACID/MULTIVIT NO.18 |
| Brand/Generic | Generic |
| Proprietary Name | PureVit DualFe Plus |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ferrous Fumarate, Polysaccharide Iron Complex |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 10; .8; 15; 53; 1; 53; 1.3; 30; 5; 6; 200; 10; 18.2 |
| Active Ingredient Units | 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 |
| Substance Name | CALCIUM PANTOTHENATE; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; IRON DEXTRAN; MANGANESE SULFATE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE |
| Labeler Name | PureTek Corporation |
| Pharmaceutical Class | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Iron [CS], Magnetic Resonance Contrast Activity [MoA], Paramagnetic Contrast Agent [EPC], Parenteral Iron Replacement [ |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59088-0112-66 (59088011266)
| NDC Package Code | 59088-112-66 |
|---|---|
| Billing NDC | 59088011266 |
| Package | 90 CAPSULE in 1 BOTTLE, PLASTIC (59088-112-66) |
| Marketing Start Date | 2011-06-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |