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NDC 59088-0172-54 Prometa 30; 120; 200; 20; 55; 45; 10; 27; 1000; 200; 2.6; 50; 20; 150; 50; 3.4; 70; 3; 1500; 25 mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1 Details
Prometa 30; 120; 200; 20; 55; 45; 10; 27; 1000; 200; 2.6; 50; 20; 150; 50; 3.4; 70; 3; 1500; 25 mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1
Prometa 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; CALCIUM CARBONATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CHROMIUM NICOTINATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; POTASSIUM IODIDE; PYRID.
Product Information
| NDC | 59088-0172 |
|---|---|
| Product ID | 59088-172_f43540c0-7416-78c3-e053-2995a90aa2d4 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Prometa |
| 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 | 30; 120; 200; 20; 55; 45; 10; 27; 1000; 200; 2.6; 50; 20; 150; 50; 3.4; 70; 3; 1500; 25 |
| Active Ingredient Units | mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/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; CALCIUM CARBONATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CHROMIUM NICOTINATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; POTASSIUM IODIDE; PYRID |
| 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 59088-0172-54 (59088017254)
| NDC Package Code | 59088-172-54 |
|---|---|
| Billing NDC | 59088017254 |
| Package | 30 TABLET in 1 BOTTLE, PLASTIC (59088-172-54) |
| Marketing Start Date | 2021-01-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |