ofloxacin
Generic: ofloxacin
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ofloxacin
Generic Name
ofloxacin
Labeler
nucare pharmaceuticals, inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
ofloxacin 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3919
Product ID
68071-3919_448425b6-3950-a860-e063-6294a90aa994
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215886
Listing Expiration
2026-12-31
Marketing Start
2023-12-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713919
Hyphenated Format
68071-3919
Supplemental Identifiers
RxCUI
UPC
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
- 5 mL in 1 BOTTLE, DROPPER (68071-3919-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "448425b6-3950-a860-e063-6294a90aa994", "openfda": {"nui": ["N0000175937", "M0023650"], "upc": ["0368071391954"], "unii": ["A4P49JAZ9H"], "rxcui": ["312075"], "spl_set_id": ["4484283c-7839-e75d-e063-6394a90a8639"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOTTLE, DROPPER (68071-3919-5)", "package_ndc": "68071-3919-5", "marketing_start_date": "20251126"}], "brand_name": "ofloxacin", "product_id": "68071-3919_448425b6-3950-a860-e063-6294a90aa994", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "68071-3919", "generic_name": "ofloxacin", "labeler_name": "NuCare 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": "20231201", "listing_expiration_date": "20261231"}