Package 68788-8449-5
Brand: ofloxacin
Generic: ofloxacinPackage Facts
Identity
Package NDC
68788-8449-5
Digits Only
6878884495
Product NDC
68788-8449
Description
1 BOTTLE, DROPPER in 1 CARTON (68788-8449-5) / 5 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
Brand
ofloxacin
Generic
ofloxacin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "58078c0a-8299-42fb-9e63-5d479a021aad", "openfda": {"nui": ["N0000175937", "M0023650"], "unii": ["A4P49JAZ9H"], "rxcui": ["312075"], "spl_set_id": ["306ed758-3c43-4f42-bd44-562ec65891dc"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (68788-8449-5) / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "68788-8449-5", "marketing_start_date": "20230525"}], "brand_name": "ofloxacin", "product_id": "68788-8449_58078c0a-8299-42fb-9e63-5d479a021aad", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "68788-8449", "generic_name": "ofloxacin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ofloxacin", "active_ingredients": [{"name": "OFLOXACIN", "strength": "3 mg/mL"}], "application_number": "ANDA215886", "marketing_category": "ANDA", "marketing_start_date": "20230525", "listing_expiration_date": "20261231"}