"0642-0096-01" National Drug Code (NDC)

NDC Code	0642-0096-01
Package Description	*1 KIT in 1 CARTON (0642-0096-01) 5 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 5 CAPSULE, LIQUID FILLED in 1 BLISTER PACK**
Product NDC	0642-0096
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Vitafol Fe Plus
Non-Proprietary Name	Vitamin A, Ascorbic Acid, Vitamin D, .alpha.-tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Iodine, Iron, Magnesium, Zinc, Copper, Doconexent, And Docusate Sodium
Dosage Form	KIT
Start Marketing Date	20151001
End Marketing Date	20230113
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Exeltis USA, Inc.