Duet DHA - 44118-807-30 - (.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)

Alphabetical Index


Drug Information of Duet DHA

Product NDC: 44118-807
Proprietary Name: Duet DHA
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
Active Ingredient(s):    & nbsp;   .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
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Duet DHA

Product NDC: 44118-807
Labeler Name: Eckson Labs, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110909

Package Information of Duet DHA

Package NDC: 44118-807-30
Package Description: 1 KIT in 1 CARTON (44118-807-30) * 30 TABLET in 1 BOTTLE (44118-803-30) * 30 CAPSULE, GELATIN COATED in 1 BOTTLE (44118-805-30)

NDC Information of Duet DHA

NDC Code 44118-807-30
Proprietary Name Duet DHA
Package Description 1 KIT in 1 CARTON (44118-807-30) * 30 TABLET in 1 BOTTLE (44118-803-30) * 30 CAPSULE, GELATIN COATED in 1 BOTTLE (44118-805-30)
Product NDC 44118-807
Product Type Name HUMAN PRESCRIPTION DRUG
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 Name KIT
Route Name ORAL
Start Marketing Date 20110909
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Eckson Labs, LLC
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Complete Information of Duet DHA


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