moxifloxacin

Generic: moxifloxacin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name moxifloxacin
Generic Name moxifloxacin
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

moxifloxacin hydrochloride 400 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-8357
Product ID 63629-8357_27864513-a113-4ec1-9e78-41bc762172bc
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 636298357
Hyphenated Format 63629-8357

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 (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
  • 7 TABLET, FILM COATED in 1 BOTTLE (63629-8357-1)
  • 10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2)
source: ndc

Packages (2)

Ingredients (1)

moxifloxacin hydrochloride (400 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "27864513-a113-4ec1-9e78-41bc762172bc", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["d20ba997-30de-445c-8766-924112bd834a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (63629-8357-1)", "package_ndc": "63629-8357-1", "marketing_start_date": "20200917"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2)", "package_ndc": "63629-8357-2", "marketing_start_date": "20201105"}], "brand_name": "Moxifloxacin", "product_id": "63629-8357_27864513-a113-4ec1-9e78-41bc762172bc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "63629-8357", "generic_name": "Moxifloxacin", "labeler_name": "Bryant Ranch Prepack", "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"}