moxifloxacin
Generic: moxifloxacin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
moxifloxacin
Generic Name
moxifloxacin
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
moxifloxacin hydrochloride 400 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636298357
Hyphenated Format
63629-8357
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 7 TABLET, FILM COATED in 1 BOTTLE (63629-8357-1)
- 10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2)
Packages (2)
Ingredients (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"}