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 50090-6609
Product ID 50090-6609_20c49868-6dc2-4951-8729-16b51689c387
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 500906609
Hyphenated Format 50090-6609

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
  • 10 TABLET, FILM COATED in 1 BOTTLE (50090-6609-0)
  • 7 TABLET, FILM COATED in 1 BOTTLE (50090-6609-1)
source: ndc

Packages (2)

50090-6609-0 10 TABLET, FILM COATED in 1 BOTTLE (50090-6609-0) 50090-6609-1 7 TABLET, FILM COATED in 1 BOTTLE (50090-6609-1)

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": "20c49868-6dc2-4951-8729-16b51689c387", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["c71e5987-edd7-4c38-b646-3e48a6e51bf4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-6609-0)", "package_ndc": "50090-6609-0", "marketing_start_date": "20230823"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (50090-6609-1)", "package_ndc": "50090-6609-1", "marketing_start_date": "20231031"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "50090-6609_20c49868-6dc2-4951-8729-16b51689c387", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-6609", "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"}