Package 51655-489-52

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 51655-489-52
Digits Only 5165548952
Product NDC 51655-489
Product ID 51655-489_490f74f0-91bc-3e85-e063-6394a90a9ef9
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-489-52)

Marketing

Marketing Status
Marketed Since 2020-12-10
Brand glimepiride
Generic glimepiride
Sample Package No

Linked Drug Pages (1)

Glimepiride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "490f74f0-91bc-3e85-e063-6394a90a9ef9", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["f3184cd3-df99-db32-e053-2995a90aa573"], "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 (51655-489-26)", "package_ndc": "51655-489-26", "marketing_start_date": "20230227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-489-52)", "package_ndc": "51655-489-52", "marketing_start_date": "20201210"}], "brand_name": "Glimepiride", "product_id": "51655-489_490f74f0-91bc-3e85-e063-6394a90a9ef9", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "51655-489", "generic_name": "Glimepiride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "4 mg/1"}], "application_number": "ANDA077091", "marketing_category": "ANDA", "marketing_start_date": "20201210", "listing_expiration_date": "20271231"}