Drugplain

Floriva 400 [iU]/mL

CHOLECALCIFEROL and SODIUM FLUORIDE · LIQUID · BonGeo Pharmaceuticals, Inc.

No Recall History
Plain English

Floriva is a liquid containing cholecalciferol and sodium fluoride at 400 [iU]/mL, taken oral. Manufactured by BonGeo Pharmaceuticals, Inc..

Key Facts

Brand Name
Floriva
Generic Name
CHOLECALCIFEROL and SODIUM FLUORIDE
NDC Code (Product)
52796-172
Manufacturer
BonGeo Pharmaceuticals, Inc.
Strength
400 [iU]/mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Drug Class
Vitamin D [EPC]
Marketing Start
10/15/2014

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug hypersensitivity2 reports
hospitalisation2 reports
surgery2 reports
acute respiratory failure1 reports
arthralgia1 reports
bacterial infection1 reports
blood pressure increased1 reports
chronic disease1 reports
complication associated with device1 reports
death1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Dosage & Administration

Directions USE AS DIRECTED BY YOUR PHYSICIAN.

Warnings

WARNING KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. IF OVERDOSAGE IS SUSPECTED, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY 1-800-222-1222. TABLET SHOULD BE CHEWED. THIS TABLET, AS WITH ALL TABLETS, IS NOT RECOMMENDED FOR CHILDREN UNDER AGE OF 4 DUE TO RISK OF CHOKING.

Frequently Asked Questions

What is Floriva used for?

Floriva contains CHOLECALCIFEROL and SODIUM FLUORIDE. It is a liquid taken oral. Consult your doctor for specific uses.

Is Floriva a controlled substance?

Floriva is not classified as a controlled substance by the DEA.

What is the generic name for Floriva?

The generic name for Floriva is CHOLECALCIFEROL and SODIUM FLUORIDE. There are no other listed brand versions of CHOLECALCIFEROL and SODIUM FLUORIDE.

What is the NDC code for Floriva 400 [iU]/mL?

The NDC (National Drug Code) for Floriva 400 [iU]/mL is 52796-172, listed by BonGeo Pharmaceuticals, Inc..

Product NDC

52796-172

Package NDC

52796-172-50

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)