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Two medicines, side by side

Alogliptin vs saxagliptin

Alogliptin and saxagliptin are both labeled for type 2 diabetes. Drugs@FDA records approvals of alogliptin since 2013 and of saxagliptin since 2009. Pharmacies paid $4.96 per alogliptin 12.5 mg tablet and $1.04 per saxagliptin HCl 5 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like.

Check it at the source: the alogliptin FDA label on DailyMed (effective February 28, 2025); the saxagliptin FDA label on DailyMed (effective January 27, 2026).

Highlights of the alogliptin record

Alogliptin (Nesina) · label of February 28, 2025

Used for

From the label: indications

NESINA ® is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. NESINA is a dipeptidyl peptidase-4 (DPP-4) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. ( 1 ) Limitations of Use: Should not be used in patients with type 1 diabetes mellitus. […]

On the market

Earliest approval on file
January 25, 2013
Generic labelers
none listed
Pharmacy cost
$4.96 per tablet

Supply and safety

Shortage
No current entry
Recalls
0

Highlights of the saxagliptin record

Saxagliptin (Onglyza) · label of January 27, 2026

Used for

From the label: indications

Saxagliptin tablets are a dipeptidyl peptidase-4 (DPP-4) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. ( 1.1 ) Limitations of use: • Not recommended for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis. […]

On the market

Earliest approval on file
July 31, 2009
Generic labelers
3 labelers
Pharmacy cost
$1.04 per tablet

Supply and safety

Shortage
No current entry
Recalls
2

Source: FDA drug labels via openFDA (Alogliptin label of February 28, 2025, Saxagliptin label of January 27, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do alogliptin and saxagliptin differ on the record?

Both are in FDA's class dipeptidyl peptidase 4 inhibitors.

Half-life, in each label's words: Alogliptin, “Elimination NESINA was eliminated with a mean terminal half-life (t 1/2 ) of approximately 21 hours.”; Saxagliptin, “Following a single oral dose of saxagliptin 5 mg to healthy subjects, the mean plasma terminal half-life (t 1/2 ) for …”

Generics: alogliptin none approved; saxagliptin since 2023 (Drugs@FDA).

AlogliptinSaxagliptin
Labeled forType 2 diabetesType 2 diabetes
Pharmacologic classDipeptidyl Peptidase 4 InhibitorDipeptidyl Peptidase 4 Inhibitor
How it works (label)Increased concentrations of the incretin hormones such as glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are released into the bloodstream from the small intestine in response to meals.Increased concentrations of the incretin hormones such as glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are released into the bloodstream from the small intestine in response to meals.
Half-life (label)Elimination NESINA was eliminated with a mean terminal half-life (t 1/2 ) of approximately 21 hours.Following a single oral dose of saxagliptin 5 mg to healthy subjects, the mean plasma terminal half-life (t 1/2 ) for saxagliptin and its active metabolite was 2.5 and 3.1 hours, respectively.
Earliest approval on file (Drugs@FDA)January 25, 2013July 31, 2009
First generic approvednoneJuly 31, 2023
Generic labelers (NDC)none listed3 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$4.96 per tablet (Alogliptin 12.5 mg tablet)$1.04 per tablet (Saxagliptin HCl 5 mg tablet)
12-month price change+9%-74%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded02
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)3,4091,458
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What next?

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