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NDC 59088-0182-58 Ribotin-E 45; 250; 100; 25; 75; 13.75; 37.5; 1; 13; 9; 500; 37.5; .75; 25; 22.5; 15; 24.5; 25; 6; 3.35; 30; 3.25; 1500; 15 mg/1; mg/1; ug/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1 Details
Ribotin-E 45; 250; 100; 25; 75; 13.75; 37.5; 1; 13; 9; 500; 37.5; .75; 25; 22.5; 15; 24.5; 25; 6; 3.35; 30; 3.25; 1500; 15 mg/1; mg/1; ug/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1
Ribotin-E is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; BIOTIN; BORON; CALCIUM CARBONATE; CHOLECALCIFEROL; CHROMIUM NICOTINATE; CUPROUS OXIDE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; PANTOTHENIC A.
Product Information
| NDC | 59088-0182 |
|---|---|
| Product ID | 59088-182_f204c835-2fb6-27b1-e053-2995a90a43b9 |
| Associated GPIs | 78310000000300 |
| GCN Sequence Number | 082130 |
| GCN Sequence Number Description | mv-mn no.89/iron/folic acid TABLET 9 MG-0.5MG ORAL |
| HIC3 | C6Z |
| HIC3 Description | MULTIVITAMIN PREPARATIONS |
| GCN | 49445 |
| HICL Sequence Number | 047250 |
| HICL Sequence Number Description | MULTIVITAMIN WITH MINERALS NO.89/FERROUS FUMARATE/FOLIC ACID |
| Brand/Generic | Brand |
| Proprietary Name | Ribotin-E |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ferrous Fumarate, Folic Acid |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 45; 250; 100; 25; 75; 13.75; 37.5; 1; 13; 9; 500; 37.5; .75; 25; 22.5; 15; 24.5; 25; 6; 3.35; 30; 3.25; 1500; 15 |
| Active Ingredient Units | mg/1; mg/1; ug/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1 |
| Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; BIOTIN; BORON; CALCIUM CARBONATE; CHOLECALCIFEROL; CHROMIUM NICOTINATE; CUPROUS OXIDE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; PANTOTHENIC A |
| Labeler Name | PureTek Corporation |
| Pharmaceutical Class | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Coagul |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59088-0182-58 (59088018258)
| NDC Package Code | 59088-182-58 |
|---|---|
| Billing NDC | 59088018258 |
| Package | 60 TABLET in 1 BOTTLE, PLASTIC (59088-182-58) |
| Marketing Start Date | 2021-02-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |