levofloxacin
Generic: levofloxacin
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
levofloxacin
Generic Name
levofloxacin
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
levofloxacin 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-085
Product ID
72789-085_40319459-b17c-0929-e063-6294a90acf2f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201043
Listing Expiration
2026-12-31
Marketing Start
2011-06-20
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789085
Hyphenated Format
72789-085
Supplemental Identifiers
RxCUI
UPC
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
ANDA201043 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-085-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40319459-b17c-0929-e063-6294a90acf2f", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0372789085500"], "unii": ["6GNT3Y5LMF"], "rxcui": ["199885"], "spl_set_id": ["b8defac4-9deb-433b-928e-0ef4ee0123a2"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-085-50)", "package_ndc": "72789-085-50", "marketing_start_date": "20200616"}], "brand_name": "Levofloxacin", "product_id": "72789-085_40319459-b17c-0929-e063-6294a90acf2f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72789-085", "generic_name": "Levofloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "500 mg/1"}], "application_number": "ANDA201043", "marketing_category": "ANDA", "marketing_start_date": "20110620", "listing_expiration_date": "20261231"}