levofloxacin
Generic: levofloxacin
Labeler: coupler llcDrug Facts
Product Profile
Brand Name
levofloxacin
Generic Name
levofloxacin
Labeler
coupler llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
levofloxacin 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67046-1078
Product ID
67046-1078_2cee69f0-e493-7eb5-e063-6394a90a4b99
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077652
Listing Expiration
2026-12-31
Marketing Start
2025-01-30
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
670461078
Hyphenated Format
67046-1078
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
ANDA077652 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1078-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cee69f0-e493-7eb5-e063-6394a90a4b99", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199884"], "spl_set_id": ["2cee61b7-be51-0fe5-e063-6294a90af9e3"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1078-3)", "package_ndc": "67046-1078-3", "marketing_start_date": "20250130"}], "brand_name": "levofloxacin", "product_id": "67046-1078_2cee69f0-e493-7eb5-e063-6394a90a4b99", "dosage_form": "TABLET, FILM COATED", "product_ndc": "67046-1078", "generic_name": "levofloxacin", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "250 mg/1"}], "application_number": "ANDA077652", "marketing_category": "ANDA", "marketing_start_date": "20250130", "listing_expiration_date": "20261231"}