moxifloxacin

Generic: moxifloxacin

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

Drug Facts

Product Profile

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

moxifloxacin hydrochloride 400 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-233
Product ID 72789-233_40ad11b9-8248-8d3f-e063-6294a90a26eb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076938
Listing Expiration 2026-12-31
Marketing Start 2014-03-05

Pharmacologic Class

Classes
fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789233
Hyphenated Format 72789-233

Supplemental Identifiers

RxCUI
311787
UPC
0372789233109
UNII
C53598599T

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 moxifloxacin (source: ndc)
Generic Name moxifloxacin (source: ndc)
Application Number ANDA076938 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)
source: ndc

Packages (1)

72789-233-10 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)

Ingredients (1)

moxifloxacin hydrochloride (400 mg/1)

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40ad11b9-8248-8d3f-e063-6294a90a26eb", "openfda": {"upc": ["0372789233109"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["1c6f7150-a8f4-408f-956f-c26d37030cf4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)", "package_ndc": "72789-233-10", "marketing_start_date": "20220215"}], "brand_name": "Moxifloxacin", "product_id": "72789-233_40ad11b9-8248-8d3f-e063-6294a90a26eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-233", "generic_name": "Moxifloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA076938", "marketing_category": "ANDA", "marketing_start_date": "20140305", "listing_expiration_date": "20261231"}