moxifloxacin

Generic: moxifloxacin

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

moxifloxacin hydrochloride 400 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-845
Product ID 31722-845_40b874c7-8b88-6a93-e063-6394a90ad44f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204836
Listing Expiration 2026-12-31
Marketing Start 2023-03-02

Pharmacologic Class

Classes
fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722845
Hyphenated Format 31722-845

Supplemental Identifiers

RxCUI
311787
UPC
0331722845304
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 (source: ndc)
Application Number ANDA204836 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (31722-845-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)
source: ndc

Packages (2)

31722-845-05 500 TABLET, FILM COATED in 1 BOTTLE (31722-845-05) 31722-845-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)

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": "40b874c7-8b88-6a93-e063-6394a90ad44f", "openfda": {"upc": ["0331722845304"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["1e6bc886-eec9-4cd8-be78-7563817457f2"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-845-05)", "package_ndc": "31722-845-05", "marketing_start_date": "20230302"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)", "package_ndc": "31722-845-30", "marketing_start_date": "20230302"}], "brand_name": "Moxifloxacin", "product_id": "31722-845_40b874c7-8b88-6a93-e063-6394a90ad44f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "31722-845", "generic_name": "Moxifloxacin", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA204836", "marketing_category": "ANDA", "marketing_start_date": "20230302", "listing_expiration_date": "20261231"}