Folixate
Generic: FOLATE, VITAMIN D3
Basic Information
Manufacturer
PureTek Corporation
Product Type
HUMAN PRESCRIPTION DRUG
Route of Administration
ORAL
FDA Set ID
0bb91f61-b61b-c894-e063-6394a90ae51c
Indications & Usage
INDICATIONS AND USAGE Folixate ™ is indicated for dietary management of patients with unique nutritional needs requiring increased folate level and Vitamin D supplementation.
Folixate™ can be taken by women of childbearing age, pregnant women, and lactating and nonlactating mothers.
Folixate™ can be taken by women of childbearing age, pregnant women, and lactating and nonlactating mothers.
Adverse Reactions
ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folate.
You should call your doctor for medical advice about serious adverse events.
To report adverse side effects or to obtain product information, contact PureTek Corporation, at 1-877-921-7873.
You should call your doctor for medical advice about serious adverse events.
To report adverse side effects or to obtain product information, contact PureTek Corporation, at 1-877-921-7873.