59088-659 NDC - LIVITA ADULTS (FOLATE, MULTIVITAMIN)

Drug Information

  • Product NDC: 59088-659
  • Proprietary Name: Livita Adults
  • Non Proprietary Name: Folate, Multivitamin
  • Active Ingredient(s): 30 mg/15mL .ALPHA.-TOCOPHEROL ACETATE, D-; 200 mg/15mL ASCORBIC ACID; 30 ug/15mL BIOTIN; 200 mg/15mL CALCIUM CITRATE; 5 mg/15mL CALCIUM PANTOTHENATE; 10 ug/15mL CHOLECALCIFEROL; 200 mg/15mL CHOLINE BITARTRATE; 500 mg/15mL INULIN; 1000 ug/15mL LEVOMEFOLATE CALCIUM; 100 mg/15mL MAGNESIUM CITRATE; 2.4 ug/15mL METHYLCOBALAMIN; 8 mg/15mL NIACINAMIDE; 1.7 mg/15mL PYRIDOXINE HYDROCHLORIDE; 1.3 mg/15mL RIBOFLAVIN; 1.2 mg/15mL THIAMINE MONONITRATE; 900 ug/15mL VITAMIN A ACETATE; 2 mg/15mL ZINC PICOLINATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): 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]

Labeler Information

Field Name Field Value
Labeler Name: PureTek Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:12/15/2023

Package Information

No. Package Code Package Description Billing Unit
159088-659-31480 mL in 1 BOTTLE (59088-659-31)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC59088-659The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELivita AdultsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEFolate, MultivitaminThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/15/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEPureTek CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME.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 PICOLINATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH30; 200; 30; 200; 5; 10; 200; 500; 1000; 100; 2.4; 8; 1.7; 1.3; 1.2; 900; 2 
ACTIVE INGRED UNITmg/15mL; mg/15mL; ug/15mL; mg/15mL; mg/15mL; ug/15mL; mg/15mL; mg/15mL; ug/15mL; mg/15mL; ug/15mL; mg/15mL; mg/15mL; mg/15mL; mg/15mL; ug/15mL; mg/15mL 
PHARM CLASSESAnalogs/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] 

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This page was last updated on: 7/4/2025

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