Folixapure is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Puretek Corporation. The primary component is Folic Acid; Vitamin D.
Product ID | 59088-163_aa1daf3a-9673-6996-e053-2a95a90a5f87 |
NDC | 59088-163 |
Product Type | Human Prescription Drug |
Proprietary Name | Folixapure |
Generic Name | Folic Acid, Vitamin D3 |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2020-07-10 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | PureTek Corporation |
Substance Name | FOLIC ACID; VITAMIN D |
Active Ingredient Strength | 1 mg/1; ug/1 |
Pharm Classes | Vitamin D [CS],Vitamin D [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2020-07-10 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
59088-163 | Folixapure | Folic Acid, Vitamin D3 |
59088-128 | DermacinRx FoliPlus D | Folic Acid, Vitamin D3 |
59088-090 | DermacinRx PureFolix | Folic Acid, Vitamin D3 |
59088-184 | DermacinRx Purefoltin | Folic Acid, Vitamin D3 |
59088-524 | Dotremin | Folic Acid, Vitamin D3 |
59088-185 | Folditam | Folic Acid, Vitamin D3 |
59088-200 | Foltamin | Folic Acid, Vitamin D3 |
59088-447 | Foltrexyl | Folic Acid, Vitamin D3 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FOLIXAPURE 90090112 not registered Live/Pending |
PureTek Corporation 2020-08-03 |