Package 51407-775-01

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-775-01
Digits Only 5140777501
Product NDC 51407-775
Product ID 51407-775_2eed2f37-4778-58f4-e063-6294a90a348e
Description

100 TABLET, FILM COATED in 1 BOTTLE (51407-775-01)

Marketing

Marketing Status
Marketed Since 2024-05-07
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": "2eed2f37-4778-58f4-e063-6294a90a348e", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511", "197512"], "spl_set_id": ["1b54c195-71ba-2523-e063-6294a90ada73"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51407-775-01)", "package_ndc": "51407-775-01", "marketing_start_date": "20240507"}], "brand_name": "Ciprofloxacin", "product_id": "51407-775_2eed2f37-4778-58f4-e063-6294a90a348e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "51407-775", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20040609", "listing_expiration_date": "20261231"}