levofloxacin

Generic: levofloxacin

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

levofloxacin 750 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-248
Product ID 72789-248_2bad21ae-f086-92a5-e063-6294a90adce0
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)
fluoroquinolone antibacterial [epc]
Chemical Structure
fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789248
Hyphenated Format 72789-248

Supplemental Identifiers

RxCUI
311296
UPC
0372789248059
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
  • 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-05)
  • 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-07)
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-10)
source: ndc

Packages (3)

72789-248-05 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-05) 72789-248-07 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-07) 72789-248-10 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-10)

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": "2bad21ae-f086-92a5-e063-6294a90adce0", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0372789248059"], "unii": ["6GNT3Y5LMF"], "rxcui": ["311296"], "spl_set_id": ["d98cf024-51fa-45a1-b247-da55aba88ca0"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-05)", "package_ndc": "72789-248-05", "marketing_start_date": "20220621"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-07)", "package_ndc": "72789-248-07", "marketing_start_date": "20220421"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-248-10)", "package_ndc": "72789-248-10", "marketing_start_date": "20220426"}], "brand_name": "Levofloxacin", "product_id": "72789-248_2bad21ae-f086-92a5-e063-6294a90adce0", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72789-248", "generic_name": "Levofloxacin", "labeler_name": "PD-Rx 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": "20150109", "listing_expiration_date": "20261231"}