Package 68071-3639-8
Brand: glimepiride
Generic: glimepiridePackage Facts
Identity
Package NDC
68071-3639-8
Digits Only
6807136398
Product NDC
68071-3639
Description
180 TABLET in 1 BOTTLE (68071-3639-8)
Marketing
Marketing Status
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": "1c336dcb-ba7c-a01b-e063-6294a90a4845", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0368071363982"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["1c335fc7-24d0-5526-e063-6394a90a488e"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (68071-3639-8)", "package_ndc": "68071-3639-8", "marketing_start_date": "20240701"}], "brand_name": "Glimepiride", "product_id": "68071-3639_1c336dcb-ba7c-a01b-e063-6294a90a4845", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68071-3639", "generic_name": "Glimepiride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glimepiride", "active_ingredients": [{"name": "GLIMEPIRIDE", "strength": "2 mg/1"}], "application_number": "ANDA202112", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20261231"}