moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name moxifloxacin hydrochloride
Generic Name moxifloxacin hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

moxifloxacin hydrochloride 400 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7244
Product ID 50090-7244_54fdd364-609d-4d3a-8f62-8bc20bf3b74e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202632
Listing Expiration 2026-12-31
Marketing Start 2014-03-04

Pharmacologic Class

Classes
fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907244
Hyphenated Format 50090-7244

Supplemental Identifiers

RxCUI
311787
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 hydrochloride (source: ndc)
Generic Name moxifloxacin hydrochloride (source: ndc)
Application Number ANDA202632 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 7 TABLET, FILM COATED in 1 BOTTLE (50090-7244-1)
source: ndc

Packages (1)

50090-7244-1 7 TABLET, FILM COATED in 1 BOTTLE (50090-7244-1)

Ingredients (1)

moxifloxacin hydrochloride (400 mg/1)

Linked Drug Pages (1)

MOXIFLOXACIN HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "54fdd364-609d-4d3a-8f62-8bc20bf3b74e", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["02c29e8e-8346-4e28-b7fc-2f4cb61ad37d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (50090-7244-1)", "package_ndc": "50090-7244-1", "marketing_start_date": "20240913"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "50090-7244_54fdd364-609d-4d3a-8f62-8bc20bf3b74e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7244", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOXIFLOXACIN HYDROCHLORIDE", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA202632", "marketing_category": "ANDA", "marketing_start_date": "20140304", "listing_expiration_date": "20261231"}