"59088-162-54" National Drug Code (NDC)

NDC Code	59088-162-54
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (59088-162-54)
Product NDC	59088-162
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Diatrol
Non-Proprietary Name	Vitamins And Mineral
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20240126
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	PureTek Corporation
Substance Name	BIOTIN; VANADYL SULFATE; CHROMIUM NICOTINATE; GYMNEMA SYLVESTRE LEAF; ARGININE HYDROCHLORIDE; .ALPHA.-TOCOPHEROL ACETATE, DL-; PHYTONADIONE; VITAMIN A; ASCORBIC ACID; CHOLECALCIFEROL; PYRIDOXINE HYDROCHLORIDE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; LEVOMEFOLATE CALCIUM; METHYLCOBALAMIN; PANTOTHENIC ACID
Strength	30; 15; 200; 100; 60; 13.5; 90; 900; 50; 18.75; 8; 4; 4; 24; 1000; 8; 8
Strength Unit	ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; ug/1; mg/1
Pharmacy Classes	Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Folate Analog [EPC], Folic Acid [CS], Increased Prothrombin Activity [PE], Nicotinic Acid [EPC], Nicotinic Acids [CS], Reversed Anticoagulation Activity [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], Vitamin K [CS], Vitamin K [EPC], Warfarin Reversal Agent [EPC]