moxifloxacin
Generic: moxifloxacin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
moxifloxacin
Generic Name
moxifloxacin
Labeler
bryant ranch prepack
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
moxifloxacin hydrochloride monohydrate 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2107
Product ID
72162-2107_5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090080
Listing Expiration
2026-12-31
Marketing Start
2017-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622107
Hyphenated Format
72162-2107
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
ANDA090080 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (72162-2107-2) / 3 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68", "openfda": {"unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["1cc031d7-0766-41c0-b5b3-35119c850e23"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (72162-2107-2) / 3 mL in 1 BOTTLE, DROPPER", "package_ndc": "72162-2107-2", "marketing_start_date": "20170701"}], "brand_name": "Moxifloxacin", "product_id": "72162-2107_5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72162-2107", "generic_name": "moxifloxacin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "5 mg/mL"}], "application_number": "ANDA090080", "marketing_category": "ANDA", "marketing_start_date": "20170701", "listing_expiration_date": "20261231"}