ciprofloxacin
Generic: ciprofolxacin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
ciprofloxacin
Generic Name
ciprofolxacin
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
ciprofloxacin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2450
Product ID
71335-2450_a5fcba51-4ab6-4b4a-a73d-64dec62a2e52
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208921
Listing Expiration
2026-12-31
Marketing Start
2023-10-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352450
Hyphenated Format
71335-2450
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 7 TABLET in 1 BOTTLE (71335-2450-0)
- 14 TABLET in 1 BOTTLE (71335-2450-1)
- 30 TABLET in 1 BOTTLE (71335-2450-2)
- 20 TABLET in 1 BOTTLE (71335-2450-3)
- 60 TABLET in 1 BOTTLE (71335-2450-4)
- 6 TABLET in 1 BOTTLE (71335-2450-5)
- 10 TABLET in 1 BOTTLE (71335-2450-6)
- 28 TABLET in 1 BOTTLE (71335-2450-7)
- 100 TABLET in 1 BOTTLE (71335-2450-8)
- 40 TABLET in 1 BOTTLE (71335-2450-9)
Packages (10)
71335-2450-0
7 TABLET in 1 BOTTLE (71335-2450-0)
71335-2450-1
14 TABLET in 1 BOTTLE (71335-2450-1)
71335-2450-2
30 TABLET in 1 BOTTLE (71335-2450-2)
71335-2450-3
20 TABLET in 1 BOTTLE (71335-2450-3)
71335-2450-4
60 TABLET in 1 BOTTLE (71335-2450-4)
71335-2450-5
6 TABLET in 1 BOTTLE (71335-2450-5)
71335-2450-6
10 TABLET in 1 BOTTLE (71335-2450-6)
71335-2450-7
28 TABLET in 1 BOTTLE (71335-2450-7)
71335-2450-8
100 TABLET in 1 BOTTLE (71335-2450-8)
71335-2450-9
40 TABLET in 1 BOTTLE (71335-2450-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a5fcba51-4ab6-4b4a-a73d-64dec62a2e52", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["2b8288a2-18bf-423c-b175-33174be729d4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE (71335-2450-0)", "package_ndc": "71335-2450-0", "marketing_start_date": "20240815"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-2450-1)", "package_ndc": "71335-2450-1", "marketing_start_date": "20240815"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2450-2)", "package_ndc": "71335-2450-2", "marketing_start_date": "20240815"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2450-3)", "package_ndc": "71335-2450-3", "marketing_start_date": "20240815"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2450-4)", "package_ndc": "71335-2450-4", "marketing_start_date": "20240815"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (71335-2450-5)", "package_ndc": "71335-2450-5", "marketing_start_date": "20240815"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2450-6)", "package_ndc": "71335-2450-6", "marketing_start_date": "20240815"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2450-7)", "package_ndc": "71335-2450-7", "marketing_start_date": "20240815"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2450-8)", "package_ndc": "71335-2450-8", "marketing_start_date": "20240815"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-2450-9)", "package_ndc": "71335-2450-9", "marketing_start_date": "20240815"}], "brand_name": "Ciprofloxacin", "product_id": "71335-2450_a5fcba51-4ab6-4b4a-a73d-64dec62a2e52", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "71335-2450", "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"}