NDC 59088-163

Folixapure

Folic Acid, Vitamin D3

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 ID59088-163_aa1daf3a-9673-6996-e053-2a95a90a5f87
NDC59088-163
Product TypeHuman Prescription Drug
Proprietary NameFolixapure
Generic NameFolic Acid, Vitamin D3
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2020-07-10
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NamePureTek Corporation
Substance NameFOLIC ACID; VITAMIN D
Active Ingredient Strength1 mg/1; ug/1
Pharm ClassesVitamin D [CS],Vitamin D [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 59088-163-54

30 TABLET in 1 BOTTLE, PLASTIC (59088-163-54)
Marketing Start Date2020-07-10
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Folixapure" or generic name "Folic Acid, Vitamin D3"

NDCBrand NameGeneric Name
59088-163FolixapureFolic Acid, Vitamin D3
59088-128DermacinRx FoliPlus DFolic Acid, Vitamin D3
59088-090DermacinRx PureFolixFolic Acid, Vitamin D3
59088-184DermacinRx PurefoltinFolic Acid, Vitamin D3
59088-524DotreminFolic Acid, Vitamin D3
59088-185FolditamFolic Acid, Vitamin D3
59088-200FoltaminFolic Acid, Vitamin D3
59088-447FoltrexylFolic Acid, Vitamin D3

Trademark Results [Folixapure]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FOLIXAPURE
FOLIXAPURE
90090112 not registered Live/Pending
PureTek Corporation
2020-08-03

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