Package 11980-779-05

Brand: ocuflox

Generic: ofloxacin
NDC Package

Package Facts

Identity

Package NDC 11980-779-05
Digits Only 1198077905
Product NDC 11980-779
Description

1 BOTTLE, DROPPER in 1 CARTON (11980-779-05) / 5 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 1993-08-01
Brand ocuflox
Generic ofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "4ba88457-b1b2-4bbc-b086-a2bab56752a0", "openfda": {"nui": ["N0000175937", "M0023650"], "unii": ["A4P49JAZ9H"], "rxcui": ["207202", "312075"], "spl_set_id": ["7aab4449-3dda-4e2c-8e40-b3244a548bf5"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (11980-779-05)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "11980-779-05", "marketing_start_date": "19930801"}], "brand_name": "OCUFLOX", "product_id": "11980-779_4ba88457-b1b2-4bbc-b086-a2bab56752a0", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "11980-779", "generic_name": "ofloxacin", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OCUFLOX", "active_ingredients": [{"name": "OFLOXACIN", "strength": "3 mg/mL"}], "application_number": "NDA019921", "marketing_category": "NDA", "marketing_start_date": "19930801", "listing_expiration_date": "20261231"}