Package 68180-422-01

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 68180-422-01
Digits Only 6818042201
Product NDC 68180-422
Description

1 BOTTLE in 1 CARTON (68180-422-01) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-07-01
Brand moxifloxacin
Generic moxifloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "40262fef-9713-4538-b96b-c44b257d6a25", "openfda": {"upc": ["0368180422013"], "unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["ae77e219-8af9-4aa4-96d3-05c9726a1d3c"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68180-422-01)  / 3 mL in 1 BOTTLE", "package_ndc": "68180-422-01", "marketing_start_date": "20170701"}], "brand_name": "Moxifloxacin", "product_id": "68180-422_40262fef-9713-4538-b96b-c44b257d6a25", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68180-422", "generic_name": "Moxifloxacin", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "5 mg/mL"}], "application_number": "ANDA202867", "marketing_category": "ANDA", "marketing_start_date": "20170701", "listing_expiration_date": "20261231"}