Package 68084-722-65

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68084-722-65
Digits Only 6808472265
Product NDC 68084-722
Product ID 68084-722_2b24dadc-fe4e-61dd-e063-6294a90a2a96
Description

50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11)

Marketing

Marketing Status
Marketed Since 2014-03-19
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": "2b24dadc-fe4e-61dd-e063-6294a90a2a96", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["1ed191f5-7df5-488c-bb72-91ac0b618d9a"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11)", "package_ndc": "68084-722-65", "marketing_start_date": "20140319"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "68084-722_2b24dadc-fe4e-61dd-e063-6294a90a2a96", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68084-722", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "American Health Packaging", "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": "20140319", "listing_expiration_date": "20261231"}