Duet DHA Balanced
- Product NDC
- 44118-750
- 11-digit product format
- 441180750
- Labeler code
- 44118
- Product ID
- 44118-750_9a9ec604-5432-635e-e053-2995a90a78d6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary 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 form
- KIT
- Labeler
- Eckson Labs, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-10-30
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44118-750-05 | 44118075005 | 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) | 1 kit | 2012-10-30 | 0000-00-00 | Yes | No | Current |
| 44118-750-30 | 44118075030 | 1 KIT in 1 CARTON (44118-750-30) * 30 TABLET in 1 BLISTER PACK (44118-751-30) * 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK (44118-752-30) | 1 kit | 2012-10-30 | 0000-00-00 | No | No | Current |