NDC 70710-1987 – Sitagliptin and metformin hydrochloride

Sitagliptin 50 mg/1; Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70710-1987

Product details

Brand name
Sitagliptin and metformin hydrochloride
Generic name
Sitagliptin and Metformin Hydrochloride
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA216743
Marketed since
March 14, 2024
Listing expires
December 31, 2027
Pharmacologic class
Biguanide; Dipeptidyl Peptidase 4 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sitagliptin and Metformin Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
70710-1987-660 TABLET, FILM COATED in 1 BOTTLE (70710-1987-6)Mar 14, 2024
70710-1987-8180 TABLET, FILM COATED in 1 BOTTLE (70710-1987-8)Mar 14, 2024

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