Package 68788-7694-3

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 68788-7694-3
Digits Only 6878876943
Product NDC 68788-7694
Description

30 TABLET in 1 BOTTLE (68788-7694-3)

Marketing

Marketing Status
Marketed Since 2020-04-01
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": "a26345dc-3c59-4778-a705-42f6caf71410", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["6KY687524K"], "rxcui": ["199246"], "spl_set_id": ["fc711cb8-49fb-4562-83e4-b8017030aee5"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7694-1)", "package_ndc": "68788-7694-1", "marketing_start_date": "20200401"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7694-3)", "package_ndc": "68788-7694-3", "marketing_start_date": "20200401"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7694-6)", "package_ndc": "68788-7694-6", "marketing_start_date": "20200401"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7694-9)", "package_ndc": "68788-7694-9", "marketing_start_date": "20200401"}], "brand_name": "Glimepiride", "product_id": "68788-7694_a26345dc-3c59-4778-a705-42f6caf71410", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68788-7694", "generic_name": "Glimepiride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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": "20200401", "listing_expiration_date": "20261231"}