NDC 59088-167 – Vitrexate
.alpha.-tocopherol Acetate, Dl- 30 mg/1; Magnesium Oxide 200 mg/1; Chromium Nicotinate 35 ug/1; Pyridoxine Hydrochloride 20 mg/1; Molybdenum 45 ug/1; Selenium… · Tablet · Oral
Product NDC59088-167
Product details
- Brand name
- Vitrexate
- Generic name
- Folic Acid
- Labeler
- PureTek Corporation
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketed since
- November 30, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Blood Coagulation Factor; Calculi Dissolution Agent; Copper Absorption Inhibitor; Osmotic Laxative; Paramagnetic Contrast Agent; Vitamin A; Vitamin B12; Vitamin B6 Analog; Vitamin C; Vitamin D
Active ingredients
- .alpha.-tocopherol Acetate, Dl- 30 mg/1
- Magnesium Oxide 200 mg/1
- Chromium Nicotinate 35 ug/1
- Pyridoxine Hydrochloride 20 mg/1
- Molybdenum 45 ug/1
- Selenium 55 ug/1
- Cholecalciferol 20 ug/1
- Riboflavin 3.4 mg/1
- Niacinamide 20 mg/1
- Ascorbic Acid 120 mg/1
- Folic Acid 1000 ug/1
- Cyanocobalamin 8 ug/1
- Calcium Carbonate 200 mg/1
- Vitamin A Acetate 1500 ug/1
- Thiamine Mononitrate 3 mg/1
- Zinc Oxide 25 mg/1
- Manganese Sulfate 2.3 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 59088-167-54 | 30 TABLET in 1 BOTTLE, PLASTIC (59088-167-54) | Nov 30, 2020 |