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Two medicines, side by side

Glipizide vs sitagliptin

Glipizide and sitagliptin are both labeled for type 2 diabetes. Drugs@FDA records approvals of glipizide since 1984 and of sitagliptin since 2006. Pharmacies paid $0.0339 per glipizide 5 mg tablet and $3.77 per sitagliptin phosphate 100 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. In FDA's classes, glipizide is a sulfonylurea and sitagliptin a dipeptidyl peptidase 4 inhibitor.

Check it at the source: the glipizide FDA label on DailyMed (effective January 8, 2026); the sitagliptin FDA label on DailyMed (effective November 14, 2024).

Highlights of the glipizide record

Glipizide (Glucotrol) · label of January 8, 2026

Used for

From the label: indications

Glipizide extended-release tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. […]

On the market

Earliest approval on file
May 8, 1984
Generic labelers
31 labelers
Pharmacy cost
$0.0339 per tablet

Supply and safety

Shortage
No current entry
Recalls
9

Highlights of the sitagliptin record

Sitagliptin (Januvia) · label of November 14, 2024

Used for

From the label: indications

JANUVIA ® is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. JANUVIA 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. […]

On the market

Earliest approval on file
October 16, 2006
Generic labelers
4 labelers
Pharmacy cost
$3.77 per tablet

Supply and safety

Shortage
No current entry
Recalls
1

Source: FDA drug labels via openFDA (Glipizide label of January 8, 2026, Sitagliptin label of November 14, 2024); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do glipizide and sitagliptin differ on the record?

In FDA's classes, glipizide is a sulfonylurea and sitagliptin a dipeptidyl peptidase 4 inhibitor.

How each works, in its label's words: Glipizide, “Glipizide primarily lowers blood glucose by stimulating the release of insulin from the pancreas, an effect dependent upon functioning beta cells in the pancreatic islets.”; Sitagliptin, “Sitagliptin is a DPP-4 inhibitor, which is believed to exert its actions in patients with type 2 diabetes mellitus by slowing the inactivation of incretin hormones.”

Half-life, in each label's words: Glipizide, “The mean terminal elimination half-life of glipizide ranged from 2 to 5 hours after single or multiple doses in …”; Sitagliptin, “Following a single oral 100-mg dose to healthy volunteers, mean plasma AUC of sitagliptin was 8.52 μM•hr, C max was 950 …”

Generics: glipizide since 1994; sitagliptin since 2025 (Drugs@FDA).

GlipizideSitagliptin
Labeled forType 2 diabetesType 2 diabetes
Pharmacologic classSulfonylureaDipeptidyl Peptidase 4 Inhibitor
How it works (label)Glipizide primarily lowers blood glucose by stimulating the release of insulin from the pancreas, an effect dependent upon functioning beta cells in the pancreatic islets.Sitagliptin is a DPP-4 inhibitor, which is believed to exert its actions in patients with type 2 diabetes mellitus by slowing the inactivation of incretin hormones.
Half-life (label)The mean terminal elimination half-life of glipizide ranged from 2 to 5 hours after single or multiple doses in patients with type 2 diabetes mellitus.Following a single oral 100-mg dose to healthy volunteers, mean plasma AUC of sitagliptin was 8.52 μM•hr, C max was 950 nM, and apparent terminal half-life (t 1/2 ) was 12.4 hours.
Earliest approval on file (Drugs@FDA)May 8, 1984October 16, 2006
First generic approvedMay 10, 1994December 29, 2025
Generic labelers (NDC)31 labelers4 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0339 per tablet (Glipizide 5 mg tablet)$3.77 per tablet (Sitagliptin phosphate 100 mg tablet)
12-month price change-2%n/a
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded91
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)60,55574,197
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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