Package 70518-4133-0

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 70518-4133-0
Digits Only 7051841330
Product NDC 70518-4133
Description

30 TABLET in 1 BLISTER PACK (70518-4133-0)

Marketing

Marketing Status
Marketed Since 2024-07-03
Brand ciprofloxacin
Generic ciprofolxacin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fa5fad1-c8f4-0048-e063-6394a90a9b99", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["4edc4fda-7834-46cc-a0ed-22f117e6e10b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4133-0)", "package_ndc": "70518-4133-0", "marketing_start_date": "20240703"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (70518-4133-1)", "package_ndc": "70518-4133-1", "marketing_start_date": "20241006"}], "brand_name": "Ciprofloxacin", "product_id": "70518-4133_3fa5fad1-c8f4-0048-e063-6394a90a9b99", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-4133", "generic_name": "Ciprofolxacin", "labeler_name": "REMEDYREPACK 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": "20240703", "listing_expiration_date": "20261231"}