Drugplain

Tilia Fe

NdAc and EE Tablets and Ferrous Fumarate Tablets · KIT · Mayne Pharma Inc.

No Recall History
Plain English

Tilia Fe is a kit containing ndac and ee tablets and ferrous fumarate tablets. Manufactured by Mayne Pharma Inc..

Key Facts

Brand Name
Tilia Fe
Generic Name
NdAc and EE Tablets and Ferrous Fumarate Tablets
NDC Code (Product)
51862-896
Manufacturer
Mayne Pharma Inc.
Dosage Form
KIT
Marketing Status
Application #
ANDA202962
Marketing Start
10/15/2020

Recall History

No Recall History

Side Effects Reported to FDA

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

gastrooesophageal reflux disease5 reports
headache4 reports
injection site pain4 reports
anxiety3 reports
diarrhoea3 reports
muscle spasms3 reports
abdominal distension2 reports
ankylosing spondylitis2 reports
arthralgia2 reports
chest pain2 reports

Frequently Asked Questions

What is Tilia Fe used for?

Tilia Fe contains NdAc and EE Tablets and Ferrous Fumarate Tablets. It is a kit taken as directed. Consult your doctor for specific uses.

Is Tilia Fe a controlled substance?

Tilia Fe is not classified as a controlled substance by the DEA.

What is the generic name for Tilia Fe?

The generic name for Tilia Fe is NdAc and EE Tablets and Ferrous Fumarate Tablets. There are no other listed brand versions of NdAc and EE Tablets and Ferrous Fumarate Tablets.

What is the NDC code for Tilia Fe ?

The NDC (National Drug Code) for Tilia Fe is 51862-896, listed by Mayne Pharma Inc..

Product NDC

51862-896

Package NDC

51862-896-01

Other Tilia Fe Dosages

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

Data from openFDA · Public domain (CC0 1.0)