alogliptin and metformin hydrochloride

Generic: alogliptin and metformin hydrochloride

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

Drug Facts

Product Profile

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

alogliptin benzoate 12.5 mg/1, metformin hydrochloride 1000 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5993
Product ID 50090-5993_58968f11-76a2-4e8d-8414-dc636614dedb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA203414
Listing Expiration 2026-12-31
Marketing Start 2016-04-08

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 500905993
Hyphenated Format 50090-5993

Supplemental Identifiers

RxCUI
1368385
UNII
EEN99869SC 786Z46389E

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 alogliptin and metformin hydrochloride (source: ndc)
Generic Name alogliptin and metformin hydrochloride (source: ndc)
Application Number NDA203414 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
  • 1000 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-5993-0)
source: ndc

Packages (1)

50090-5993-0 90 TABLET, FILM COATED in 1 BOTTLE (50090-5993-0)

Ingredients (2)

alogliptin benzoate (12.5 mg/1) metformin hydrochloride (1000 mg/1)

Linked Drug Pages (1)

alogliptin and metformin hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "58968f11-76a2-4e8d-8414-dc636614dedb", "openfda": {"unii": ["EEN99869SC", "786Z46389E"], "rxcui": ["1368385"], "spl_set_id": ["9112d6b9-4771-4194-886d-7db887470bcc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5993-0)", "package_ndc": "50090-5993-0", "marketing_start_date": "20220610"}], "brand_name": "alogliptin and metformin hydrochloride", "product_id": "50090-5993_58968f11-76a2-4e8d-8414-dc636614dedb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "50090-5993", "generic_name": "alogliptin and metformin hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "alogliptin and metformin hydrochloride", "active_ingredients": [{"name": "ALOGLIPTIN BENZOATE", "strength": "12.5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "NDA203414", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160408", "listing_expiration_date": "20261231"}