Package 72189-334-05

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 72189-334-05
Digits Only 7218933405
Product NDC 72189-334
Product ID 72189-334_2c3d95a4-32d2-ef3b-e063-6294a90ac144
Description

3 mL in 1 BOTTLE (72189-334-05)

Marketing

Marketing Status
Marketed Since 2022-03-08
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": "2c3d95a4-32d2-ef3b-e063-6294a90ac144", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["d9b6a460-6377-76d0-e053-2995a90a3d05"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "3 mL in 1 BOTTLE (72189-334-05)", "package_ndc": "72189-334-05", "marketing_start_date": "20220308"}], "brand_name": "MOXIFLOXACIN", "product_id": "72189-334_2c3d95a4-32d2-ef3b-e063-6294a90ac144", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-334", "generic_name": "MOXIFLOXACIN", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOXIFLOXACIN", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA202916", "marketing_category": "ANDA", "marketing_start_date": "20220308", "listing_expiration_date": "20261231"}