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NDC 44118-0807-30 Duet DHA Details
Duet DHA
Duet DHA is a ORAL KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eckson Labs, LLC. The primary component is .
Product Information
| NDC | 44118-0807 |
|---|---|
| Product ID | 44118-807_04c70e1e-a02c-879a-e063-6394a90a13fb |
| Associated GPIs | 78512097006318 |
| GCN Sequence Number | 069502 |
| GCN Sequence Number Description | prenatal vit106/iron/folic/om3 COMBO. PKG 25-1-400MG ORAL |
| HIC3 | C6F |
| HIC3 Description | PRENATAL VITAMIN PREPARATIONS |
| GCN | 32579 |
| HICL Sequence Number | 039248 |
| HICL Sequence Number Description | PRENATAL VITS 106/SOD FEREDETATE-IRON PS/FOLIC ACID/OMEGA-3S |
| Brand/Generic | Brand |
| Proprietary Name | Duet DHA |
| Proprietary Name Suffix | 400 |
| 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, IODIN |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | KIT |
| Route | ORAL |
| Active Ingredient Strength | n/a |
| Active Ingredient Units | n/a |
| Substance Name | n/a |
| Labeler Name | Eckson Labs, LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | n/a |
Package
NDC 44118-0807-30 (44118080730)
| NDC Package Code | 44118-807-30 |
|---|---|
| Billing NDC | 44118080730 |
| Package | 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 Date | 2011-09-09 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |