Package 68788-7864-4

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 68788-7864-4
Digits Only 6878878644
Product NDC 68788-7864
Description

40 TABLET, FILM COATED in 1 BOTTLE (68788-7864-4)

Marketing

Marketing Status
Marketed Since 2021-02-08
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "77f966b6-f1ac-4e1d-8937-a10f72241d5a", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["f45294bd-e01b-4e21-af82-c788ec73f79a"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68788-7864-0)", "package_ndc": "68788-7864-0", "marketing_start_date": "20210208"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68788-7864-1)", "package_ndc": "68788-7864-1", "marketing_start_date": "20210208"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-7864-2)", "package_ndc": "68788-7864-2", "marketing_start_date": "20210208"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7864-3)", "package_ndc": "68788-7864-3", "marketing_start_date": "20210208"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (68788-7864-4)", "package_ndc": "68788-7864-4", "marketing_start_date": "20210208"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, DROPPER (68788-7864-6)", "package_ndc": "68788-7864-6", "marketing_start_date": "20210208"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68788-7864-8)", "package_ndc": "68788-7864-8", "marketing_start_date": "20210208"}], "brand_name": "Ciprofloxacin", "product_id": "68788-7864_77f966b6-f1ac-4e1d-8937-a10f72241d5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68788-7864", "generic_name": "Ciprofloxacin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20210208", "listing_expiration_date": "20261231"}