Package 60687-860-01

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-860-01
Digits Only 6068786001
Product NDC 60687-860
Description

100 BLISTER PACK in 1 CARTON (60687-860-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-860-11)

Marketing

Marketing Status
Discontinued 2028-02-29
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f27c2c4-b732-19a4-e063-6394a90a4105", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["0fac4466-fbe5-49d2-96e3-e3ac2739bd5b"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-860-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-860-11)", "package_ndc": "60687-860-01", "marketing_end_date": "20280229", "marketing_start_date": "20240930"}], "brand_name": "Ciprofloxacin", "product_id": "60687-860_3f27c2c4-b732-19a4-e063-6394a90a4105", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "60687-860", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20280229", "marketing_start_date": "20240930"}