moxifloxacin ophthalmic solution
Generic: moxifloxacin ophthalmic
Labeler: fosun pharma usa inc.Drug Facts
Product Profile
Brand Name
moxifloxacin ophthalmic solution
Generic Name
moxifloxacin ophthalmic
Labeler
fosun pharma usa inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
moxifloxacin hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72266-158
Product ID
72266-158_3a227739-e57d-10aa-e063-6294a90ac95e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208778
Listing Expiration
2026-12-31
Marketing Start
2020-08-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72266158
Hyphenated Format
72266-158
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 ophthalmic solution (source: ndc)
Generic Name
moxifloxacin ophthalmic (source: ndc)
Application Number
ANDA208778 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (72266-158-01) / 3 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "3a227739-e57d-10aa-e063-6294a90ac95e", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["9eae534a-9253-4a45-9ab7-2543626f49e6"], "manufacturer_name": ["Fosun Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72266-158-01) / 3 mL in 1 BOTTLE", "package_ndc": "72266-158-01", "marketing_start_date": "20200824"}], "brand_name": "Moxifloxacin Ophthalmic Solution", "product_id": "72266-158_3a227739-e57d-10aa-e063-6294a90ac95e", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72266-158", "generic_name": "Moxifloxacin Ophthalmic", "labeler_name": "Fosun Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Ophthalmic Solution", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA208778", "marketing_category": "ANDA", "marketing_start_date": "20200824", "listing_expiration_date": "20261231"}