Package 85766-023-05

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 85766-023-05
Digits Only 8576602305
Product NDC 85766-023
Description

1 BOTTLE, PLASTIC in 1 CARTON (85766-023-05) / 5 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2025-08-05
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "4a166fe1-3a63-544a-e063-6294a90ab5be", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["190395a8-c05f-4e31-9a89-7af6428ebbb9"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (85766-023-05)  / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "85766-023-05", "marketing_start_date": "20250805"}], "brand_name": "ciprofloxacin", "product_id": "85766-023_4a166fe1-3a63-544a-e063-6294a90ab5be", "dosage_form": "SOLUTION", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "85766-023", "generic_name": "Ciprofloxacin", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "ANDA077568", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20271231"}