Package 76420-331-03

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-331-03
Digits Only 7642033103
Product NDC 76420-331
Description

1 BOTTLE, PLASTIC in 1 CARTON (76420-331-03) / 3 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2025-04-19
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "331b69c5-5ad7-a90a-e063-6394a90acfd6", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["8f92f110-32d6-4d0c-a415-7a9a4cafb9b8"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (76420-331-03)  / 3 mL in 1 BOTTLE, PLASTIC", "package_ndc": "76420-331-03", "marketing_start_date": "20250419"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "76420-331_331b69c5-5ad7-a90a-e063-6394a90acfd6", "dosage_form": "SOLUTION", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "76420-331", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA212616", "marketing_category": "ANDA", "marketing_start_date": "20210210", "listing_expiration_date": "20261231"}