ofloxacin
Generic: ofloxacin
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
ofloxacin
Generic Name
ofloxacin
Labeler
preferred pharmaceuticals inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
ofloxacin 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8449
Product ID
68788-8449_58078c0a-8299-42fb-9e63-5d479a021aad
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215886
Listing Expiration
2026-12-31
Marketing Start
2023-05-25
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888449
Hyphenated Format
68788-8449
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ofloxacin (source: ndc)
Generic Name
ofloxacin (source: ndc)
Application Number
ANDA215886 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (68788-8449-5) / 5 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
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"}