United States · FDA National Drug Code directory
Sitagliptin and metformin hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70710-1987_6c6865d9-b997-4c50-bb00-0b188ae0d2c0
- Product NDC
- 70710-1987
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sitagliptin and Metformin Hydrochloride
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20240314
- Source listing expiry
- 20271231
Source-listed ingredients
- SITAGLIPTIN — 50 mg/1
- METFORMIN HYDROCHLORIDE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (70710-1987-6) · 70710-1987-6
- 180 TABLET, FILM COATED in 1 BOTTLE (70710-1987-8) · 70710-1987-8
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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