Package 58657-676-01

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 58657-676-01
Digits Only 5865767601
Product NDC 58657-676
Product ID 58657-676_41b40647-01ce-1916-e063-6394a90aaadd
Description

100 TABLET, COATED in 1 BOTTLE (58657-676-01)

Marketing

Marketing Status
Marketed Since 2020-08-12
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": "41b40647-01ce-1916-e063-6394a90aaadd", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511", "309309"], "spl_set_id": ["acb03e72-ce94-58c5-e053-2a95a90a683a"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (58657-676-01)", "package_ndc": "58657-676-01", "marketing_start_date": "20200812"}], "brand_name": "Ciprofloxacin", "product_id": "58657-676_41b40647-01ce-1916-e063-6394a90aaadd", "dosage_form": "TABLET, COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "58657-676", "generic_name": "Ciprofloxacin", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20200812", "listing_expiration_date": "20261231"}