Package 0904-7407-04

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7407-04
Digits Only 0904740704
Product NDC 0904-7407
Product ID 0904-7407_eeab280e-fdca-45ae-b2ae-325799c9c3ff
Description

30 BLISTER PACK in 1 CARTON (0904-7407-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-03-08
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

MOXIFLOXACIN HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eeab280e-fdca-45ae-b2ae-325799c9c3ff", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["815d71cf-02de-4190-9bd1-3fdc67ef0f06"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7407-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7407-04", "marketing_start_date": "20240308"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7407-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7407-06", "marketing_start_date": "20240308"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "0904-7407_eeab280e-fdca-45ae-b2ae-325799c9c3ff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "0904-7407", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOXIFLOXACIN HYDROCHLORIDE", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA202632", "marketing_category": "ANDA", "marketing_start_date": "20240308", "listing_expiration_date": "20261231"}