Package 51655-565-26

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 51655-565-26
Digits Only 5165556526
Product NDC 51655-565
Description

90 TABLET in 1 BOTTLE, PLASTIC (51655-565-26)

Marketing

Marketing Status
Marketed Since 2021-01-25
Brand glimepiride
Generic glimepiride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "494e0a81-2169-be71-e063-6394a90aded0", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["dae404ac-881a-14d8-e053-2995a90acd41"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-565-26)", "package_ndc": "51655-565-26", "marketing_start_date": "20210125"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-565-52)", "package_ndc": "51655-565-52", "marketing_start_date": "20230227"}], "brand_name": "Glimepiride", "product_id": "51655-565_494e0a81-2169-be71-e063-6394a90aded0", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "51655-565", "generic_name": "Glimepiride", "labeler_name": "Northwind Health Company, LLC", "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": "20210125", "listing_expiration_date": "20271231"}