Package 70518-2837-4

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 70518-2837-4
Digits Only 7051828374
Product NDC 70518-2837
Product ID 70518-2837_4ab6c45a-7fe1-1d11-e063-6394a90a7bbd
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-4)

Marketing

Marketing Status
Marketed Since 2023-02-05
Brand ciprofloxacin
Generic ciprofloxacin
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": "4ab6c45a-7fe1-1d11-e063-6394a90a7bbd", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["c08b37c3-5f01-47ed-9508-02813bbd008b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-4)", "package_ndc": "70518-2837-4", "marketing_start_date": "20230205"}], "brand_name": "Ciprofloxacin", "product_id": "70518-2837_4ab6c45a-7fe1-1d11-e063-6394a90a7bbd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-2837", "generic_name": "Ciprofloxacin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20200818", "listing_expiration_date": "20271231"}