Package 68788-8875-1

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 68788-8875-1
Digits Only 6878888751
Product NDC 68788-8875
Description

14 TABLET in 1 BOTTLE (68788-8875-1)

Marketing

Marketing Status
Marketed Since 2025-05-19
Brand ciprofloxacin
Generic ciprofolxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15755a35-e29a-47c1-89ab-e6645bb3ade9", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["15755a35-e29a-47c1-89ab-e6645bb3ade9"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (68788-8875-0)", "package_ndc": "68788-8875-0", "marketing_start_date": "20250519"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-8875-1)", "package_ndc": "68788-8875-1", "marketing_start_date": "20250519"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8875-2)", "package_ndc": "68788-8875-2", "marketing_start_date": "20250519"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8875-3)", "package_ndc": "68788-8875-3", "marketing_start_date": "20250519"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68788-8875-4)", "package_ndc": "68788-8875-4", "marketing_start_date": "20250519"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8875-6)", "package_ndc": "68788-8875-6", "marketing_start_date": "20250519"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (68788-8875-8)", "package_ndc": "68788-8875-8", "marketing_start_date": "20250519"}], "brand_name": "Ciprofloxacin", "product_id": "68788-8875_15755a35-e29a-47c1-89ab-e6645bb3ade9", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68788-8875", "generic_name": "Ciprofolxacin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20250519", "listing_expiration_date": "20261231"}