Package 70518-4229-6

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 70518-4229-6
Digits Only 7051842296
Product NDC 70518-4229
Description

30 TABLET in 1 BLISTER PACK (70518-4229-6)

Marketing

Marketing Status
Marketed Since 2025-07-31
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": "495de50d-93b8-0884-e063-6294a90a9996", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["c527d138-e32c-418f-9573-a3d8a796279f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-0)", "package_ndc": "70518-4229-0", "marketing_start_date": "20241111"}, {"sample": false, "description": "20 TABLET in 1 BLISTER PACK (70518-4229-1)", "package_ndc": "70518-4229-1", "marketing_start_date": "20241211"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2)", "package_ndc": "70518-4229-2", "marketing_start_date": "20250114"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4229-3)", "package_ndc": "70518-4229-3", "marketing_start_date": "20250129"}, {"sample": false, "description": "14 TABLET in 1 BLISTER PACK (70518-4229-4)", "package_ndc": "70518-4229-4", "marketing_start_date": "20250519"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5)", "package_ndc": "70518-4229-5", "marketing_start_date": "20250709"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4229-6)", "package_ndc": "70518-4229-6", "marketing_start_date": "20250731"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7)", "package_ndc": "70518-4229-7", "marketing_start_date": "20260126"}], "brand_name": "Ciprofloxacin", "product_id": "70518-4229_495de50d-93b8-0884-e063-6294a90a9996", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-4229", "generic_name": "Ciprofolxacin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20241111", "listing_expiration_date": "20271231"}