Drugplain

Famotidine 20 mg 20 mg/1

Famotidine 20 mg · TABLET, COATED · MARKSANS PHARMA LIMITED

No Recall History
Plain English

Famotidine 20 mg is a tablet, coated containing famotidine 20 mg at 20 mg/1, taken oral. Manufactured by MARKSANS PHARMA LIMITED.

Key Facts

Brand Name
Famotidine 20 mg
Generic Name
Famotidine 20 mg
NDC Code (Product)
25000-087
Manufacturer
MARKSANS PHARMA LIMITED
Strength
20 mg/1
Dosage Form
TABLET, COATED
Route
ORAL
Marketing Status
Application #
ANDA217543
Drug Class
Histamine-2 Receptor Antagonist [EPC]
Marketing Start
03/10/2023

Recall History

No Recall History

Side Effects Reported to FDA

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

nausea8 reports
drug ineffective7 reports
pain5 reports
infusion related reaction4 reports
vomiting4 reports
adverse event3 reports
dizziness3 reports
fall3 reports
headache3 reports
product substitution issue3 reports

Frequently Asked Questions

What is Famotidine 20 mg used for?

Famotidine 20 mg contains Famotidine 20 mg. It is a tablet, coated taken oral. Consult your doctor for specific uses.

Is Famotidine 20 mg a controlled substance?

Famotidine 20 mg is not classified as a controlled substance by the DEA.

What is the generic name for Famotidine 20 mg?

The generic name for Famotidine 20 mg is Famotidine 20 mg. There are 1 other brand versions of Famotidine 20 mg.

What is the NDC code for Famotidine 20 mg 20 mg/1?

The NDC (National Drug Code) for Famotidine 20 mg 20 mg/1 is 25000-087, listed by MARKSANS PHARMA LIMITED.

Product NDC

25000-087

Package NDC

25000-087-03

Other Famotidine 20 mg Dosages

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

Data from openFDA · Public domain (CC0 1.0)