Package 60760-690-10

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 60760-690-10
Digits Only 6076069010
Product NDC 60760-690
Product ID 60760-690_348e9276-54df-fa85-e063-6394a90a5d26
Description

10 TABLET in 1 BOTTLE, PLASTIC (60760-690-10)

Marketing

Marketing Status
Marketed Since 2025-05-07
Brand ciprofloxacin
Generic ciprofolxacin
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": "348e9276-54df-fa85-e063-6394a90a5d26", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["348e810c-e572-f3d2-e063-6394a90a0855"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (60760-690-10)", "package_ndc": "60760-690-10", "marketing_start_date": "20250507"}], "brand_name": "Ciprofloxacin", "product_id": "60760-690_348e9276-54df-fa85-e063-6394a90a5d26", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "60760-690", "generic_name": "Ciprofolxacin", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20231001", "listing_expiration_date": "20261231"}