glimepiride
Generic: glimepiride
Labeler: avpakDrug Facts
Product Profile
Brand Name
glimepiride
Generic Name
glimepiride
Labeler
avpak
Dosage Form
TABLET
Routes
Active Ingredients
glimepiride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-359
Product ID
50268-359_4860dfbf-405a-6b0f-e063-6394a90af79c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077091
Listing Expiration
2027-12-31
Marketing Start
2019-10-02
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268359
Hyphenated Format
50268-359
Supplemental Identifiers
RxCUI
UNII
NUI
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
- 2 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-359-15) / 1 TABLET in 1 BLISTER PACK (50268-359-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4860dfbf-405a-6b0f-e063-6394a90af79c", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199245", "199246", "199247"], "spl_set_id": ["93f1e064-fcbd-e8fd-e053-2995a90a5dbb"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-359-15) / 1 TABLET in 1 BLISTER PACK (50268-359-11)", "package_ndc": "50268-359-15", "marketing_start_date": "20191002"}], "brand_name": "Glimepiride", "product_id": "50268-359_4860dfbf-405a-6b0f-e063-6394a90af79c", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50268-359", "generic_name": "Glimepiride", "labeler_name": "AvPAK", "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": "20191002", "listing_expiration_date": "20271231"}