janumet

Generic: sitagliptin and metformin hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name janumet
Generic Name sitagliptin and metformin hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 1000 mg/1, sitagliptin phosphate 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5502
Product ID 50090-5502_7511c56d-21ea-4bad-89b9-62329c2e3d75
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022044
Listing Expiration 2026-12-31
Marketing Start 2007-03-30

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs] dipeptidyl peptidase 4 inhibitor [epc] dipeptidyl peptidase 4 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905502
Hyphenated Format 50090-5502

Supplemental Identifiers

RxCUI
861771 2709488
UNII
786Z46389E TS63EW8X6F

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 janumet (source: ndc)
Generic Name sitagliptin and metformin hydrochloride (source: ndc)
Application Number NDA022044 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
  • 50 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-5502-0)
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-5502-1)
source: ndc

Packages (2)

Ingredients (2)

metformin hydrochloride (1000 mg/1) sitagliptin phosphate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7511c56d-21ea-4bad-89b9-62329c2e3d75", "openfda": {"unii": ["786Z46389E", "TS63EW8X6F"], "rxcui": ["861771", "2709488"], "spl_set_id": ["c603b844-2019-4ef4-8385-7bc3f96a2565"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-5502-0)", "package_ndc": "50090-5502-0", "marketing_start_date": "20210331"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-5502-1)", "package_ndc": "50090-5502-1", "marketing_start_date": "20230719"}], "brand_name": "JANUMET", "product_id": "50090-5502_7511c56d-21ea-4bad-89b9-62329c2e3d75", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "50090-5502", "generic_name": "SITAGLIPTIN and METFORMIN HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "JANUMET", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}, {"name": "SITAGLIPTIN PHOSPHATE", "strength": "50 mg/1"}], "application_number": "NDA022044", "marketing_category": "NDA", "marketing_start_date": "20070330", "listing_expiration_date": "20261231"}