glimepiride

Generic: glimepiride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glimepiride
Generic Name glimepiride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glimepiride 2 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-641
Product ID 63187-641_539f397e-9afb-444a-ac5b-c26f4bd791ba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078181
Listing Expiration 2026-12-31
Marketing Start 2007-08-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187641
Hyphenated Format 63187-641

Supplemental Identifiers

RxCUI
199246
UPC
0363187641306
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 ANDA078181 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63187-641-30)
  • 60 TABLET in 1 BOTTLE (63187-641-60)
  • 90 TABLET in 1 BOTTLE (63187-641-90)
source: ndc

Packages (3)

Ingredients (1)

glimepiride (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "539f397e-9afb-444a-ac5b-c26f4bd791ba", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0363187641306"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["beb0cefb-807b-4cc3-ada2-7a8ed4aa8f2b"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-641-30)", "package_ndc": "63187-641-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-641-60)", "package_ndc": "63187-641-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-641-90)", "package_ndc": "63187-641-90", "marketing_start_date": "20181201"}], "brand_name": "Glimepiride", "product_id": "63187-641_539f397e-9afb-444a-ac5b-c26f4bd791ba", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "63187-641", "generic_name": "Glimepiride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA078181", "marketing_category": "ANDA", "marketing_start_date": "20070823", "listing_expiration_date": "20261231"}