Package 73473-903-30

Brand: moxifloxacin

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 73473-903-30
Digits Only 7347390330
Product NDC 73473-903
Product ID 73473-903_45ce210f-125d-12f6-e063-6394a90a9f9b
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30)

Marketing

Marketing Status
Marketed Since 2025-12-12
Brand moxifloxacin
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45ce210f-125d-12f6-e063-6394a90a9f9b", "openfda": {"upc": ["0373473903308"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["45ce14e5-98b8-296b-e063-6294a90a769b"], "manufacturer_name": ["Solaris Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30)", "package_ndc": "73473-903-30", "marketing_start_date": "20251212"}], "brand_name": "Moxifloxacin", "product_id": "73473-903_45ce210f-125d-12f6-e063-6394a90a9f9b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "73473-903", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "Solaris Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA206295", "marketing_category": "ANDA", "marketing_start_date": "20251212", "listing_expiration_date": "20261231"}