- Product NDC
- 59088-660
- 11-digit product format
- 590880660
- Labeler code
- 59088
- Product ID
- 59088-660_297c5a87-4e85-4833-e063-6294a90a0e4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folate, Multivitamin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-12-18
- Substance
- .ALPHA.-TOCOPHEROL ACETATE, D-; ASCORBIC ACID; BIOTIN; CALCIUM CITRATE; CALCIUM PANTOTHENATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; INULIN; LEVOMEFOLATE CALCIUM; MAGNESIUM CITRATE; METHYLCOBALAMIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; VITAMIN A ACETATE; ZINC PICOLINATE
- Active strength
- 10; 66.67; 10; 66.67; 1.67; 3.33; 66.67; 166.67; 333; 33.33; .8; 2.67; .57; .43; .4; 300; .67 mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; ug/mL; mg/mL; mg/mL; mg/mL; mg/mL; ug/mL; mg/mL
- Pharmacologic classes
- 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], Folate Analog [EPC], Folic Acid [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin A [CS], Vitamin A [EPC], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes