Package 72266-158-01

Brand: moxifloxacin ophthalmic solution

Generic: moxifloxacin ophthalmic
NDC Package

Package Facts

Identity

Package NDC 72266-158-01
Digits Only 7226615801
Product NDC 72266-158
Description

1 BOTTLE in 1 CARTON (72266-158-01) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-08-24
Brand moxifloxacin ophthalmic solution
Generic moxifloxacin ophthalmic
Sample Package No

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"}