Package 68071-2228-6

Brand: glimepiride

Generic: glimepiride
NDC Package

Package Facts

Identity

Package NDC 68071-2228-6
Digits Only 6807122286
Product NDC 68071-2228
Description

60 TABLET in 1 BOTTLE (68071-2228-6)

Marketing

Marketing Status
Marketed Since 2020-07-31
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": "1d7632a7-0f26-9e5d-e063-6294a90ad21f", "openfda": {"nui": ["N0000175608", "M0020795"], "upc": ["0368071222869"], "unii": ["6KY687524K"], "rxcui": ["199247"], "spl_set_id": ["abc187f1-8645-23e9-e053-2a95a90a64a7"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-2228-6)", "package_ndc": "68071-2228-6", "marketing_start_date": "20200731"}], "brand_name": "Glimepiride", "product_id": "68071-2228_1d7632a7-0f26-9e5d-e063-6294a90ad21f", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68071-2228", "generic_name": "Glimepiride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20051006", "listing_expiration_date": "20261231"}