NDC 44118-807

Duet DHA 400

.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

Duet DHA 400 is a Oral Kit in the Human Prescription Drug category. It is labeled and distributed by Eckson Labs, Llc. The primary component is .

Product ID44118-807_60ccbdf2-942e-3f1e-e053-2a91aa0ac993
NDC44118-807
Product TypeHuman Prescription Drug
Proprietary NameDuet DHA 400
Generic 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 FormKit
Route of AdministrationORAL
Marketing Start Date2011-09-09
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameEckson Labs, LLC
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 44118-807-30

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)
Marketing Start Date2011-09-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 44118-807-30 [44118080730]

Duet DHA 400 KIT
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-09-09

Drug Details

OpenFDA Data

SPL SET ID:9532f8de-115c-4f37-9148-2e6899800f65
Manufacturer

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