levofloxacin

Generic: levofloxacin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levofloxacin
Generic Name levofloxacin
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

levofloxacin 750 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-234
Product ID 71205-234_1d9c3263-38b0-47a4-ba6f-f553254fc442
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200839
Listing Expiration 2026-12-31
Marketing Start 2012-03-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205234
Hyphenated Format 71205-234

Supplemental Identifiers

RxCUI
311296
UPC
0371205234072
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 ANDA200839 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 5 TABLET, FILM COATED in 1 BOTTLE (71205-234-05)
  • 7 TABLET, FILM COATED in 1 BOTTLE (71205-234-07)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71205-234-10)
  • 15 TABLET, FILM COATED in 1 BOTTLE (71205-234-15)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-234-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-234-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-234-90)
source: ndc

Packages (7)

71205-234-05 5 TABLET, FILM COATED in 1 BOTTLE (71205-234-05) 71205-234-07 7 TABLET, FILM COATED in 1 BOTTLE (71205-234-07) 71205-234-10 10 TABLET, FILM COATED in 1 BOTTLE (71205-234-10) 71205-234-15 15 TABLET, FILM COATED in 1 BOTTLE (71205-234-15) 71205-234-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-234-30) 71205-234-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-234-60) 71205-234-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-234-90)

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": "1d9c3263-38b0-47a4-ba6f-f553254fc442", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0371205234072"], "unii": ["6GNT3Y5LMF"], "rxcui": ["311296"], "spl_set_id": ["960fabb4-6156-4600-9a0f-7c24a89e9a31"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE (71205-234-05)", "package_ndc": "71205-234-05", "marketing_start_date": "20190301"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71205-234-07)", "package_ndc": "71205-234-07", "marketing_start_date": "20190301"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-234-10)", "package_ndc": "71205-234-10", "marketing_start_date": "20190301"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71205-234-15)", "package_ndc": "71205-234-15", "marketing_start_date": "20190301"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-234-30)", "package_ndc": "71205-234-30", "marketing_start_date": "20190301"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-234-60)", "package_ndc": "71205-234-60", "marketing_start_date": "20190301"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-234-90)", "package_ndc": "71205-234-90", "marketing_start_date": "20190301"}], "brand_name": "Levofloxacin", "product_id": "71205-234_1d9c3263-38b0-47a4-ba6f-f553254fc442", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71205-234", "generic_name": "Levofloxacin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "750 mg/1"}], "application_number": "ANDA200839", "marketing_category": "ANDA", "marketing_start_date": "20120322", "listing_expiration_date": "20261231"}