Package 61442-116-05

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 61442-116-05
Digits Only 6144211605
Product NDC 61442-116
Product ID 61442-116_2386d706-9dab-4ae0-e063-6394a90a8a06
Description

500 TABLET in 1 BOTTLE (61442-116-05)

Marketing

Marketing Status
Marketed Since 2012-01-01
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": "2386d706-9dab-4ae0-e063-6394a90a8a06", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199245", "199246", "199247"], "spl_set_id": ["72d88c6d-2f0a-4bf8-aa7f-1e1811794187"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Carlsbad Technology, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (61442-116-01)", "package_ndc": "61442-116-01", "marketing_start_date": "20120101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (61442-116-05)", "package_ndc": "61442-116-05", "marketing_start_date": "20120101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (61442-116-10)", "package_ndc": "61442-116-10", "marketing_start_date": "20120101"}], "brand_name": "Glimepiride", "product_id": "61442-116_2386d706-9dab-4ae0-e063-6394a90a8a06", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "61442-116", "generic_name": "Glimepiride", "labeler_name": "Carlsbad Technology, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA077911", "marketing_category": "ANDA", "marketing_start_date": "20120101", "listing_expiration_date": "20261231"}