glimepiride
Generic: glimepiride
Labeler: dr. reddy's laboratories limitedDrug Facts
Product Profile
Brand Name
glimepiride
Generic Name
glimepiride
Labeler
dr. reddy's laboratories limited
Dosage Form
TABLET
Routes
Active Ingredients
glimepiride 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55111-320
Product ID
55111-320_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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55111320
Hyphenated Format
55111-320
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (55111-320-01)
- 500 TABLET in 1 BOTTLE (55111-320-05)
- 30 TABLET in 1 BOTTLE (55111-320-30)
- 100 BLISTER PACK in 1 CARTON (55111-320-78) / 1 TABLET in 1 BLISTER PACK (55111-320-79)
Packages (4)
Ingredients (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 (55111-320-01)", "package_ndc": "55111-320-01", "marketing_start_date": "20051006"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-320-05)", "package_ndc": "55111-320-05", "marketing_start_date": "20051006"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-320-30)", "package_ndc": "55111-320-30", "marketing_start_date": "20051006"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (55111-320-78) / 1 TABLET in 1 BLISTER PACK (55111-320-79)", "package_ndc": "55111-320-78", "marketing_start_date": "20051006"}], "brand_name": "Glimepiride", "product_id": "55111-320_e3d50334-9896-b2f9-a481-8383eb84b16a", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "55111-320", "generic_name": "Glimepiride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "1 mg/1"}], "application_number": "ANDA077091", "marketing_category": "ANDA", "marketing_start_date": "20051006", "listing_expiration_date": "20261231"}