"44118-800-30" National Drug Code (NDC)

NDC Code	44118-800-30
Package Description	*1 KIT in 1 CARTON (44118-800-30) 30 TABLET in 1 BLISTER PACK (44118-801-30) * 30 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (44118-802-30)**
Product NDC	44118-800
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Duet Dha Balanced
Non-Proprietary Name	.beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, D-, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium Carbonate, Iron, Magnesium Oxide, Zinc Oxide, Cupric Oxide, Iodine, Omega-3 Fatty Acids
Dosage Form	KIT
Usage	ORAL
Start Marketing Date	20121030
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Eckson Labs, LLC