zituvimet

Generic: sitagliptin and metformin hydrochloride

Labeler: zydus pharmaceuticals (usa) inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zituvimet
Generic Name sitagliptin and metformin hydrochloride
Labeler zydus pharmaceuticals (usa) inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1, sitagliptin 50 mg/1

Manufacturer
Zydus Pharmaceuticals (USA) Inc.

Identifiers & Regulatory

Product NDC 70710-1786
Product ID 70710-1786_a33d6fab-1e72-4153-9f24-8a781e838f94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA216743
Listing Expiration 2026-12-31
Marketing Start 2024-03-14

Pharmacologic Class

Established (EPC)
dipeptidyl peptidase 4 inhibitor [epc]
Mechanism of Action
dipeptidyl peptidase 4 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101786
Hyphenated Format 70710-1786

Supplemental Identifiers

RxCUI
861769 861819 2677162 2677164
UNII
QFP0P1DV7Z 786Z46389E
NUI
N0000175913 N0000175912

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zituvimet (source: ndc)
Generic Name sitagliptin and metformin hydrochloride (source: ndc)
Application Number NDA216743 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 50 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (70710-1786-6)
  • 180 TABLET, FILM COATED in 1 BOTTLE (70710-1786-8)
source: ndc

Packages (2)

Ingredients (2)

metformin hydrochloride (500 mg/1) sitagliptin (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a33d6fab-1e72-4153-9f24-8a781e838f94", "openfda": {"nui": ["N0000175913", "N0000175912"], "unii": ["QFP0P1DV7Z", "786Z46389E"], "rxcui": ["861769", "861819", "2677162", "2677164"], "spl_set_id": ["eeda90a0-4941-4716-8684-f9f12cbdf3af"], "pharm_class_epc": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]"], "pharm_class_moa": ["Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (70710-1786-6)", "package_ndc": "70710-1786-6", "marketing_start_date": "20240314"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (70710-1786-8)", "package_ndc": "70710-1786-8", "marketing_start_date": "20240314"}], "brand_name": "ZITUVIMET", "product_id": "70710-1786_a33d6fab-1e72-4153-9f24-8a781e838f94", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "70710-1786", "generic_name": "Sitagliptin and Metformin Hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZITUVIMET", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}, {"name": "SITAGLIPTIN", "strength": "50 mg/1"}], "application_number": "NDA216743", "marketing_category": "NDA", "marketing_start_date": "20240314", "listing_expiration_date": "20261231"}