Package 65862-603-30

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-603-30
Digits Only 6586260330
Product NDC 65862-603
Description

30 TABLET, FILM COATED in 1 BOTTLE (65862-603-30)

Marketing

Marketing Status
Marketed Since 2014-03-04
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "412cb5bf-66ad-4815-bf15-8d225c09260b", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["d6789c17-4a2f-4519-9060-e3b0dba422f0"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-603-30)", "package_ndc": "65862-603-30", "marketing_start_date": "20140304"}, {"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (65862-603-55)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (65862-603-10)", "package_ndc": "65862-603-55", "marketing_start_date": "20140304"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-603-99)", "package_ndc": "65862-603-99", "marketing_start_date": "20140304"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "65862-603_412cb5bf-66ad-4815-bf15-8d225c09260b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "65862-603", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "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": "20140304", "listing_expiration_date": "20261231"}