moxifloxacin

Generic: moxifloxacin hydrochloride

Labeler: solaris pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name moxifloxacin
Generic Name moxifloxacin hydrochloride
Labeler solaris pharma corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

moxifloxacin hydrochloride 400 mg/1

Manufacturer
Solaris Pharma Corporation

Identifiers & Regulatory

Product NDC 73473-903
Product ID 73473-903_45ce210f-125d-12f6-e063-6394a90a9f9b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206295
Listing Expiration 2026-12-31
Marketing Start 2025-12-12

Pharmacologic Class

Classes
fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73473903
Hyphenated Format 73473-903

Supplemental Identifiers

RxCUI
311787
UPC
0373473903308
UNII
C53598599T

Packaging Origin

Original Packager
true

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 hydrochloride (source: ndc)
Application Number ANDA206295 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30)
source: ndc

Packages (1)

73473-903-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30)

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": "45ce210f-125d-12f6-e063-6394a90a9f9b", "openfda": {"upc": ["0373473903308"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["45ce14e5-98b8-296b-e063-6294a90a769b"], "manufacturer_name": ["Solaris Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30)", "package_ndc": "73473-903-30", "marketing_start_date": "20251212"}], "brand_name": "Moxifloxacin", "product_id": "73473-903_45ce210f-125d-12f6-e063-6394a90a9f9b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "73473-903", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "Solaris Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA206295", "marketing_category": "ANDA", "marketing_start_date": "20251212", "listing_expiration_date": "20261231"}