Prometa 30 mg/1
Ferrous Fumarate, Folic Acid · TABLET · PureTek Corporation
No Recall History
Plain English
Prometa is a tablet containing ferrous fumarate, folic acid at 30 mg/1, taken oral. Manufactured by PureTek Corporation.
Key Facts
- Brand Name
- Prometa
- Generic Name
- Ferrous Fumarate, Folic Acid
- NDC Code (Product)
59088-172- Manufacturer
- PureTek Corporation
- Strength
- 30 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Drug Class
- Vitamin C [EPC]; Vitamin D [EPC]
- Marketing Start
- 01/11/2021
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
diarrhoea2 reports
alcohol abuse1 reports
alopecia1 reports
arthralgia1 reports
atrial fibrillation1 reports
blood creatinine increased1 reports
blood urea increased1 reports
calciphylaxis1 reports
cataract1 reports
cerebral ischaemia1 reports
Frequently Asked Questions
What is Prometa used for?
Prometa contains Ferrous Fumarate, Folic Acid. It is a tablet taken oral. Consult your doctor for specific uses.
Is Prometa a controlled substance?
Prometa is not classified as a controlled substance by the DEA.
What is the generic name for Prometa?
The generic name for Prometa is Ferrous Fumarate, Folic Acid. There are 11 other brand versions of Ferrous Fumarate, Folic Acid.
What is the NDC code for Prometa 30 mg/1?
The NDC (National Drug Code) for Prometa 30 mg/1 is 59088-172, listed by PureTek Corporation.