Package 65862-076-01

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-076-01
Digits Only 6586207601
Product NDC 65862-076
Product ID 65862-076_9e7eb1ac-3e09-4b4c-8ce1-ab16c3102a10
Description

100 TABLET, FILM COATED in 1 BOTTLE (65862-076-01)

Marketing

Marketing Status
Discontinued 2027-01-31
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
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": "9e7eb1ac-3e09-4b4c-8ce1-ab16c3102a10", "openfda": {"upc": ["0365862076304", "0365862078506", "0365862077301"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["2b3b6a9f-259c-4736-b88f-f49d1eb64286"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-076-01)", "package_ndc": "65862-076-01", "marketing_end_date": "20270131", "marketing_start_date": "20070426"}], "brand_name": "Ciprofloxacin", "product_id": "65862-076_9e7eb1ac-3e09-4b4c-8ce1-ab16c3102a10", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "65862-076", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20070426"}