glimepiride

Generic: glimepiride

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

Drug Facts

Product Profile

Brand Name glimepiride
Generic Name glimepiride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glimepiride 4 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6322
Product ID 50090-6322_f6d891ed-a372-4f20-b4d3-a77f3af53d71
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202759
Listing Expiration 2026-12-31
Marketing Start 2012-06-29

Pharmacologic Class

Established (EPC)
sulfonylurea [epc]
Chemical Structure
sulfonylurea compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906322
Hyphenated Format 50090-6322

Supplemental Identifiers

RxCUI
199247
UNII
6KY687524K
NUI
N0000175608 M0020795

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 glimepiride (source: ndc)
Generic Name glimepiride (source: ndc)
Application Number ANDA202759 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6322-0)
  • 100 TABLET in 1 BOTTLE (50090-6322-1)
  • 60 TABLET in 1 BOTTLE (50090-6322-2)
  • 90 TABLET in 1 BOTTLE (50090-6322-3)
  • 180 TABLET in 1 BOTTLE (50090-6322-4)
source: ndc

Packages (5)

50090-6322-0 30 TABLET in 1 BOTTLE (50090-6322-0) 50090-6322-1 100 TABLET in 1 BOTTLE (50090-6322-1) 50090-6322-2 60 TABLET in 1 BOTTLE (50090-6322-2) 50090-6322-3 90 TABLET in 1 BOTTLE (50090-6322-3) 50090-6322-4 180 TABLET in 1 BOTTLE (50090-6322-4)

Ingredients (1)

glimepiride (4 mg/1)

Linked Drug Pages (1)

Glimepiride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f6d891ed-a372-4f20-b4d3-a77f3af53d71", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["a11680ba-2750-43ab-a1b1-a52ebe3e139f"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6322-0)", "package_ndc": "50090-6322-0", "marketing_start_date": "20230110"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6322-1)", "package_ndc": "50090-6322-1", "marketing_start_date": "20230110"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6322-2)", "package_ndc": "50090-6322-2", "marketing_start_date": "20230110"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6322-3)", "package_ndc": "50090-6322-3", "marketing_start_date": "20230110"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-6322-4)", "package_ndc": "50090-6322-4", "marketing_start_date": "20230110"}], "brand_name": "Glimepiride", "product_id": "50090-6322_f6d891ed-a372-4f20-b4d3-a77f3af53d71", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-6322", "generic_name": "Glimepiride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "4 mg/1"}], "application_number": "ANDA202759", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}