NDC 44118-750

Duet DHA Balanced

.beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol, D-, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium Carbonate, Iron, Magnesium, Zinc Oxide, Sodium Selenate, Cupric Oxide, Iodine, Choline, Omega-3 Fatty Acids

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

Product ID44118-750_60c8daea-0a2d-a274-e053-2a91aa0aba42
NDC44118-750
Product TypeHuman Prescription Drug
Proprietary NameDuet DHA Balanced
Generic Name.beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol, D-, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium Carbonate, Iron, Magnesium, Zinc Oxide, Sodium Selenate, Cupric Oxide, Iodine, Choline, Omega-3 Fatty Acids
Dosage FormKit
Marketing Start Date2012-10-30
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameEckson Labs, LLC
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 44118-750-05

1 KIT in 1 CARTON (44118-750-05) * 30 TABLET in 1 BLISTER PACK (44118-751-30) * 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (44118-752-30)
Marketing Start Date2012-10-30
NDC Exclude FlagN
Sample Package?Y

NDC SPL Data Element Entries

NDC 44118-750-05 [44118075005]

Duet DHA Balanced KIT
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-10-30

NDC 44118-750-30 [44118075030]

Duet DHA Balanced KIT
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-10-30

Drug Details

OpenFDA Data

SPL SET ID:f7445e81-8ae7-47fb-81c0-6b14837edbe4
Manufacturer

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