"59088-022-54" National Drug Code (NDC)

NDC Code	59088-022-54
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (59088-022-54)
Product NDC	59088-022
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Boostervite
Non-Proprietary Name	Multivitamin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20260619
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	PureTek Corporation
Substance Name	FERROUS FUMARATE; PANTOTHENIC ACID; ORANGE JUICE; BIOTIN; RIBOFLAVIN; NIACINAMIDE; ASCORBIC ACID; LEVOMEFOLATE CALCIUM; METHYLCOBALAMIN; THIAMINE MONONITRATE; PYRIDOXINE HYDROCHLORIDE; CHOLECALCIFEROL; BROCCOLI SPROUT; PRUNUS CERASUS (BITTER CHERRY) FRUIT EXTRACT; KALE; WITHANIA SOMNIFERA ROOT
Strength	100; 300; 2.5; 10; 18; 2.5; 1000; 100; 10; 2.5; 50; 2.5; 10; 10; 10; 60
Strength Unit	mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
Pharmacy Classes	Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Folate Analog [EPC], Folic Acid [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]