ciprofloxacin

Generic: ciprofolxacin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofolxacin
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2425
Product ID 72162-2425_54fb9efb-e34f-4d04-922b-c80eeb1c1200
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208921
Listing Expiration 2026-12-31
Marketing Start 2023-10-01

Pharmacologic Class

Classes
cytochrome p450 1a2 inhibitors [moa] fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622425
Hyphenated Format 72162-2425

Supplemental Identifiers

RxCUI
309309
UNII
4BA73M5E37

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ciprofloxacin (source: ndc)
Generic Name ciprofolxacin (source: ndc)
Application Number ANDA208921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-2425-1)
  • 20 TABLET in 1 BOTTLE (72162-2425-2)
  • 30 TABLET in 1 BOTTLE (72162-2425-3)
  • 28 TABLET in 1 BOTTLE (72162-2425-4)
  • 500 TABLET in 1 BOTTLE (72162-2425-5)
source: ndc

Packages (5)

72162-2425-1 100 TABLET in 1 BOTTLE (72162-2425-1) 72162-2425-2 20 TABLET in 1 BOTTLE (72162-2425-2) 72162-2425-3 30 TABLET in 1 BOTTLE (72162-2425-3) 72162-2425-4 28 TABLET in 1 BOTTLE (72162-2425-4) 72162-2425-5 500 TABLET in 1 BOTTLE (72162-2425-5)

Ingredients (1)

ciprofloxacin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "54fb9efb-e34f-4d04-922b-c80eeb1c1200", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["ab16bacd-f73f-462e-82b2-b0abb1c49cec"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2425-1)", "package_ndc": "72162-2425-1", "marketing_start_date": "20241112"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (72162-2425-2)", "package_ndc": "72162-2425-2", "marketing_start_date": "20241112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2425-3)", "package_ndc": "72162-2425-3", "marketing_start_date": "20241112"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (72162-2425-4)", "package_ndc": "72162-2425-4", "marketing_start_date": "20241112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2425-5)", "package_ndc": "72162-2425-5", "marketing_start_date": "20241112"}], "brand_name": "Ciprofloxacin", "product_id": "72162-2425_54fb9efb-e34f-4d04-922b-c80eeb1c1200", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72162-2425", "generic_name": "Ciprofolxacin", "labeler_name": "Bryant Ranch Prepack", "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": "20231001", "listing_expiration_date": "20261231"}