Package 60687-860-01
Brand: ciprofloxacin
Generic: ciprofloxacin hydrochloridePackage 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
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"}