"72988-0012-1" National Drug Code (NDC)

NDC Code	72988-0012-1
Package Description	20 TABLET in 1 PACKAGE (72988-0012-1)
Product NDC	72988-0012
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Yobisin
Non-Proprietary Name	Rehmannia Root, Angelica Gigas Root
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190422
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Lydia Co., Ltd.
Substance Name	AKEBIA STEM; ALISMA PLANTAGO-AQUATICA ROOT; ANGELICA GIGAS ROOT; CHINESE CINNAMON; FORSYTHIA SUSPENSA FRUIT; GINGER; LICORICE; PLANTAGO SEED; REHMANNIA GLUTINOSA ROOT; RHUBARB; SCUTELLARIA BAICALENSIS ROOT
Strength	416.7; 250; 416.7; 16.7; 16.7; 16.7; 125; 250; 416.7; 16.7; 250
Strength Unit	mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
Pharmacy Classes	Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS]