levofloxacin
Generic: levofloxacin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
levofloxacin
Generic Name
levofloxacin
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
levofloxacin 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0434
Product ID
71335-0434_fb951968-65db-479b-b313-2ac274ea0df2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202801
Listing Expiration
2026-12-31
Marketing Start
2015-01-09
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350434
Hyphenated Format
71335-0434
Supplemental Identifiers
RxCUI
UNII
NUI
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
levofloxacin (source: ndc)
Generic Name
levofloxacin (source: ndc)
Application Number
ANDA202801 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0434-0)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0434-1)
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-0434-2)
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-0434-3)
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-0434-4)
- 5 TABLET, FILM COATED in 1 BOTTLE (71335-0434-5)
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-0434-6)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0434-7)
- 3 TABLET, FILM COATED in 1 BOTTLE (71335-0434-8)
- 50 TABLET, FILM COATED in 1 BOTTLE (71335-0434-9)
Packages (10)
71335-0434-0
90 TABLET, FILM COATED in 1 BOTTLE (71335-0434-0)
71335-0434-1
30 TABLET, FILM COATED in 1 BOTTLE (71335-0434-1)
71335-0434-2
10 TABLET, FILM COATED in 1 BOTTLE (71335-0434-2)
71335-0434-3
7 TABLET, FILM COATED in 1 BOTTLE (71335-0434-3)
71335-0434-4
14 TABLET, FILM COATED in 1 BOTTLE (71335-0434-4)
71335-0434-5
5 TABLET, FILM COATED in 1 BOTTLE (71335-0434-5)
71335-0434-6
20 TABLET, FILM COATED in 1 BOTTLE (71335-0434-6)
71335-0434-7
60 TABLET, FILM COATED in 1 BOTTLE (71335-0434-7)
71335-0434-8
3 TABLET, FILM COATED in 1 BOTTLE (71335-0434-8)
71335-0434-9
50 TABLET, FILM COATED in 1 BOTTLE (71335-0434-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fb951968-65db-479b-b313-2ac274ea0df2", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199885"], "spl_set_id": ["804ec547-5b89-4fd0-89b3-7445543e563e"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0434-0)", "package_ndc": "71335-0434-0", "marketing_start_date": "20240403"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0434-1)", "package_ndc": "71335-0434-1", "marketing_start_date": "20180507"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-0434-2)", "package_ndc": "71335-0434-2", "marketing_start_date": "20180419"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71335-0434-3)", "package_ndc": "71335-0434-3", "marketing_start_date": "20180905"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71335-0434-4)", "package_ndc": "71335-0434-4", "marketing_start_date": "20180305"}, {"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE (71335-0434-5)", "package_ndc": "71335-0434-5", "marketing_start_date": "20180330"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-0434-6)", "package_ndc": "71335-0434-6", "marketing_start_date": "20180213"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0434-7)", "package_ndc": "71335-0434-7", "marketing_start_date": "20180214"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (71335-0434-8)", "package_ndc": "71335-0434-8", "marketing_start_date": "20220310"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (71335-0434-9)", "package_ndc": "71335-0434-9", "marketing_start_date": "20210421"}], "brand_name": "Levofloxacin", "product_id": "71335-0434_fb951968-65db-479b-b313-2ac274ea0df2", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71335-0434", "generic_name": "Levofloxacin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "500 mg/1"}], "application_number": "ANDA202801", "marketing_category": "ANDA", "marketing_start_date": "20150109", "listing_expiration_date": "20261231"}