Package 72189-321-05

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 72189-321-05
Digits Only 7218932105
Product NDC 72189-321
Product ID 72189-321_2c3d2dfe-0fff-b986-e063-6294a90a84c9
Description

3 mL in 1 BOTTLE (72189-321-05)

Marketing

Marketing Status
Marketed Since 2022-02-07
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": "2c3d2dfe-0fff-b986-e063-6294a90a84c9", "openfda": {"unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["d771e69b-7d9b-13fa-e053-2995a90ac161"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "3 mL in 1 BOTTLE (72189-321-05)", "package_ndc": "72189-321-05", "marketing_start_date": "20220207"}], "brand_name": "MOXIFLOXACIN", "product_id": "72189-321_2c3d2dfe-0fff-b986-e063-6294a90a84c9", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-321", "generic_name": "MOXIFLOXACIN", "labeler_name": "Direct Rx", "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": "20220207", "listing_expiration_date": "20261231"}