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 1 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7187
Product ID 50090-7187_b18bab5f-8b2c-4685-8c0e-aa6486d67a08
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202112
Listing Expiration 2026-12-31
Marketing Start 2023-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907187
Hyphenated Format 50090-7187

Supplemental Identifiers

RxCUI
199245
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 ANDA202112 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7187-0)
  • 100 TABLET in 1 BOTTLE (50090-7187-1)
  • 90 TABLET in 1 BOTTLE (50090-7187-2)
source: ndc

Packages (3)

50090-7187-0 30 TABLET in 1 BOTTLE (50090-7187-0) 50090-7187-1 100 TABLET in 1 BOTTLE (50090-7187-1) 50090-7187-2 90 TABLET in 1 BOTTLE (50090-7187-2)

Ingredients (1)

glimepiride (1 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": "b18bab5f-8b2c-4685-8c0e-aa6486d67a08", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199245"], "spl_set_id": ["49bf2d48-efa8-487b-b861-0124c3a4c951"], "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 (50090-7187-0)", "package_ndc": "50090-7187-0", "marketing_start_date": "20240701"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7187-1)", "package_ndc": "50090-7187-1", "marketing_start_date": "20240701"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7187-2)", "package_ndc": "50090-7187-2", "marketing_start_date": "20240701"}], "brand_name": "Glimepiride", "product_id": "50090-7187_b18bab5f-8b2c-4685-8c0e-aa6486d67a08", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50090-7187", "generic_name": "Glimepiride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "1 mg/1"}], "application_number": "ANDA202112", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20261231"}