glimepiride

Generic: glimepiride

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name glimepiride
Generic Name glimepiride
Labeler dr. reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

glimepiride 2 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-321
Product ID 55111-321_e3d50334-9896-b2f9-a481-8383eb84b16a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077091
Listing Expiration 2026-12-31
Marketing Start 2005-10-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111321
Hyphenated Format 55111-321

Supplemental Identifiers

RxCUI
199245 199246 199247
UNII
6KY687524K
NUI
N0000175608 M0020795

Packaging Origin

Original Packager
true

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 ANDA077091 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (55111-321-01)
  • 500 TABLET in 1 BOTTLE (55111-321-05)
  • 30 TABLET in 1 BOTTLE (55111-321-30)
  • 100 BLISTER PACK in 1 CARTON (55111-321-78) / 1 TABLET in 1 BLISTER PACK (55111-321-79)
source: ndc

Packages (4)

Ingredients (1)

glimepiride (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3d50334-9896-b2f9-a481-8383eb84b16a", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199245", "199246", "199247"], "spl_set_id": ["07ad4366-4b21-f633-49f3-c2b35f88168d"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-321-01)", "package_ndc": "55111-321-01", "marketing_start_date": "20051006"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-321-05)", "package_ndc": "55111-321-05", "marketing_start_date": "20051006"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-321-30)", "package_ndc": "55111-321-30", "marketing_start_date": "20051006"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (55111-321-78)  / 1 TABLET in 1 BLISTER PACK (55111-321-79)", "package_ndc": "55111-321-78", "marketing_start_date": "20051006"}], "brand_name": "Glimepiride", "product_id": "55111-321_e3d50334-9896-b2f9-a481-8383eb84b16a", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "55111-321", "generic_name": "Glimepiride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA077091", "marketing_category": "ANDA", "marketing_start_date": "20051006", "listing_expiration_date": "20261231"}