Package 72162-2107-2

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 72162-2107-2
Digits Only 7216221072
Product NDC 72162-2107
Product ID 72162-2107_5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68
Description

1 BOTTLE, DROPPER in 1 CARTON (72162-2107-2) / 3 mL in 1 BOTTLE, DROPPER

Marketing

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

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.95)

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"}