alogliptin
Generic: alogliptin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
alogliptin
Generic Name
alogliptin
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
alogliptin benzoate 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5574
Product ID
50090-5574_b2747bb4-79a6-4e24-aa7c-79fe610523e1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA022271
Listing Expiration
2026-12-31
Marketing Start
2016-04-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905574
Hyphenated Format
50090-5574
Supplemental Identifiers
RxCUI
UNII
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 (source: ndc)
Generic Name
alogliptin (source: ndc)
Application Number
NDA022271 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-5574-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b2747bb4-79a6-4e24-aa7c-79fe610523e1", "openfda": {"unii": ["EEN99869SC"], "rxcui": ["1368006"], "spl_set_id": ["38d30e4f-4212-4f7a-96b5-74b277b56cba"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5574-0)", "package_ndc": "50090-5574-0", "marketing_start_date": "20210702"}], "brand_name": "Alogliptin", "product_id": "50090-5574_b2747bb4-79a6-4e24-aa7c-79fe610523e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "50090-5574", "generic_name": "Alogliptin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alogliptin", "active_ingredients": [{"name": "ALOGLIPTIN BENZOATE", "strength": "25 mg/1"}], "application_number": "NDA022271", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160408", "listing_expiration_date": "20261231"}