Package 70518-4214-1

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4214-1
Digits Only 7051842141
Product NDC 70518-4214
Product ID 70518-4214_3ff68934-fd4f-449c-e063-6394a90a465f
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)

Marketing

Marketing Status
Marketed Since 2024-10-25
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff68934-fd4f-449c-e063-6394a90a465f", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["47d1e4c5-f669-4aca-9e8c-0d6bb833b859"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0)", "package_ndc": "70518-4214-0", "marketing_start_date": "20241015"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)", "package_ndc": "70518-4214-1", "marketing_start_date": "20241025"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2)", "package_ndc": "70518-4214-2", "marketing_start_date": "20241113"}], "brand_name": "Ciprofloxacin", "product_id": "70518-4214_3ff68934-fd4f-449c-e063-6394a90a465f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-4214", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20241015", "listing_expiration_date": "20261231"}