Package 75834-120-05

Brand: ofloxacin

Generic: ofloxacin
NDC Package

Package Facts

Identity

Package NDC 75834-120-05
Digits Only 7583412005
Product NDC 75834-120
Description

500 TABLET, COATED in 1 BOTTLE (75834-120-05)

Marketing

Marketing Status
Marketed Since 2016-07-15
Brand ofloxacin
Generic ofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "67a823b3-3e2d-4483-98e5-99fbddc0c8f5", "openfda": {"nui": ["N0000175937", "M0023650"], "upc": ["0375834112503", "0375834119502", "0375834120508"], "unii": ["A4P49JAZ9H"], "rxcui": ["198048", "198049", "198050"], "spl_set_id": ["ee1bf431-97fa-4aba-9cc3-0cfcea779ca2"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["Nivagen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (75834-120-01)", "package_ndc": "75834-120-01", "marketing_start_date": "20160715"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (75834-120-05)", "package_ndc": "75834-120-05", "marketing_start_date": "20160715"}, {"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (75834-120-50)", "package_ndc": "75834-120-50", "marketing_start_date": "20160715"}], "brand_name": "OFLOXACIN", "product_id": "75834-120_67a823b3-3e2d-4483-98e5-99fbddc0c8f5", "dosage_form": "TABLET, COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "75834-120", "generic_name": "OFLOXACIN", "labeler_name": "Nivagen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OFLOXACIN", "active_ingredients": [{"name": "OFLOXACIN", "strength": "200 mg/1"}], "application_number": "ANDA091656", "marketing_category": "ANDA", "marketing_start_date": "20160715", "listing_expiration_date": "20261231"}