Folet DHA is a Kit in the Human Prescription Drug category. It is labeled and distributed by Pronova Corporation. The primary component is .
Product ID | 67555-153_b2ade83e-2dee-43e2-be8f-2e0a39057bba |
NDC | 67555-153 |
Product Type | Human Prescription Drug |
Proprietary Name | Folet DHA |
Generic Name | Dha (docosahexaenoic Acid), Vit.a (beta-carotine), Vit.c (ascorbic Acid), Vit.d-3 (cholecalciferol), Vit.e (d-alpha-tocopheryl Acetate), Vit.b-1 (thiamine Hcl), Vit.b-2 (riboflavin), Vit.b-3 (niacinamide), Vit.b-6 (pyridoxine Hcl), Folate (1.85 Mg (6s)-5-methyltetrahydrofolate-quatrefolic), Vit.b-12 (cyanocobalamin), Iron (carbonyl Iron -ferronyl And Ferrous Bis-glycinate Chelate -ferrochel), Magnesium (magnesium Oxide), Zinc (zinc Bis-glycinate Chelate -traacs), Selenium (sodium Selenate), Docusate Sodium |
Dosage Form | Kit |
Marketing Start Date | 2014-08-28 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Pronova Corporation |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2014-08-28 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-08-28 |
Marketing End Date | 2017-03-15 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-02-18 |
SPL SET ID: | 19df5244-1a40-4f9e-af28-e2a90d996566 |
Manufacturer | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
Mark Image Registration | Serial | Company Trademark Application Date |
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![]() FOLET DHA 86334618 5008574 Live/Registered |
Pronova Corporation 2014-07-11 |