levofloxacin

Generic: levofloxacin

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levofloxacin
Generic Name levofloxacin
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

levofloxacin 750 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-8340
Product ID 68788-8340_e6558ffd-be92-4443-a351-990c571aaef7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202801
Listing Expiration 2026-12-31
Marketing Start 2023-02-02

Pharmacologic Class

Established (EPC)
fluoroquinolone antibacterial [epc]
Chemical Structure
fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888340
Hyphenated Format 68788-8340

Supplemental Identifiers

RxCUI
311296
UNII
6GNT3Y5LMF
NUI
N0000193223 M0372253

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (68788-8340-1)
  • 20 TABLET, FILM COATED in 1 BOTTLE (68788-8340-2)
  • 14 TABLET, FILM COATED in 1 BOTTLE (68788-8340-4)
  • 7 TABLET, FILM COATED in 1 BOTTLE (68788-8340-7)
source: ndc

Packages (4)

68788-8340-1 10 TABLET, FILM COATED in 1 BOTTLE (68788-8340-1) 68788-8340-2 20 TABLET, FILM COATED in 1 BOTTLE (68788-8340-2) 68788-8340-4 14 TABLET, FILM COATED in 1 BOTTLE (68788-8340-4) 68788-8340-7 7 TABLET, FILM COATED in 1 BOTTLE (68788-8340-7)

Ingredients (1)

levofloxacin (750 mg/1)

Linked Drug Pages (1)

Levofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e6558ffd-be92-4443-a351-990c571aaef7", "openfda": {"nui": ["N0000193223", "M0372253"], "unii": ["6GNT3Y5LMF"], "rxcui": ["311296"], "spl_set_id": ["2a8676a9-247f-4fdb-b644-e9785d98771f"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68788-8340-1)", "package_ndc": "68788-8340-1", "marketing_start_date": "20230202"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8340-2)", "package_ndc": "68788-8340-2", "marketing_start_date": "20230202"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68788-8340-4)", "package_ndc": "68788-8340-4", "marketing_start_date": "20230202"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (68788-8340-7)", "package_ndc": "68788-8340-7", "marketing_start_date": "20230202"}], "brand_name": "Levofloxacin", "product_id": "68788-8340_e6558ffd-be92-4443-a351-990c571aaef7", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68788-8340", "generic_name": "Levofloxacin", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "750 mg/1"}], "application_number": "ANDA202801", "marketing_category": "ANDA", "marketing_start_date": "20230202", "listing_expiration_date": "20261231"}