Drugplain

Sitagliptin Phosphate 25 mg/1

Sitagliptin Phosphate · TABLET, FILM COATED · Sandoz Inc

1 Recall on Record
Plain English

Sitagliptin phosphate is an oral tablet used to help control blood sugar levels in people with type 2 diabetes. It works by increasing the amount of insulin your body produces when blood sugar is high.

Key Facts

Brand Name
Sitagliptin Phosphate
Generic Name
Sitagliptin Phosphate
NDC Code (Product)
0781-5766
Manufacturer
Sandoz Inc
Strength
25 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA202387
Marketing Start
01/14/2026

Recall History

1 Recall on Record
Class II07/02/2013

Aidapak Services, LLC

Labeling: Label Mixup: sitaGLIPtin PHOSPHATE, Tablet, 50 mg may be potentially mis-labeled as one of the following drugs: LACTOBACILLUS, Tablet, 0 mg, NDC 64980012950, Pedigree: AD62992_1, EXP: 5/23/2014; CYANOCOBALAMIN, Tablet, 500 mcg, NDC 00536355101, Pedigree: W002860, EXP: 6/7/2014.

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

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

nausea149 reports
diarrhoea121 reports
vomiting111 reports
diabetes mellitus inadequate control110 reports
hypoglycaemia107 reports
fatigue101 reports
blood glucose increased99 reports
malaise97 reports
pyrexia95 reports
asthenia93 reports

Frequently Asked Questions

What is Sitagliptin Phosphate used for?

Sitagliptin phosphate is an oral tablet used to help control blood sugar levels in people with type 2 diabetes. It works by increasing the amount of insulin your body produces when blood sugar is high.

Is Sitagliptin Phosphate a controlled substance?

Sitagliptin Phosphate is not classified as a controlled substance by the DEA.

What is the generic name for Sitagliptin Phosphate?

The generic name for Sitagliptin Phosphate is Sitagliptin Phosphate. There are no other listed brand versions of Sitagliptin Phosphate.

What is the NDC code for Sitagliptin Phosphate 25 mg/1?

The NDC (National Drug Code) for Sitagliptin Phosphate 25 mg/1 is 0781-5766, listed by Sandoz Inc.

Product NDC

0781-5766

Package NDC

0781-5766-31

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

Data from openFDA · Public domain (CC0 1.0)