ofloxacin
Generic: ofloxacin
Labeler: nucare pharmceuticals,inc.Drug Facts
Product Profile
Brand Name
ofloxacin
Generic Name
ofloxacin
Labeler
nucare pharmceuticals,inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
ofloxacin 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3566
Product ID
68071-3566_102c825b-af5d-42e7-e063-6394a90a81a1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076513
Listing Expiration
2026-12-31
Marketing Start
2019-03-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713566
Hyphenated Format
68071-3566
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
ANDA076513 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (68071-3566-1) / 10 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": "102c825b-af5d-42e7-e063-6394a90a81a1", "openfda": {"nui": ["N0000175937", "M0023650"], "upc": ["0368071356618"], "unii": ["A4P49JAZ9H"], "rxcui": ["312075"], "spl_set_id": ["102c825b-af5c-42e7-e063-6394a90a81a1"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["NuCare Pharmceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (68071-3566-1) / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "68071-3566-1", "marketing_start_date": "20240130"}], "brand_name": "Ofloxacin", "product_id": "68071-3566_102c825b-af5d-42e7-e063-6394a90a81a1", "dosage_form": "SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "68071-3566", "generic_name": "ofloxacin", "labeler_name": "NuCare Pharmceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ofloxacin", "active_ingredients": [{"name": "OFLOXACIN", "strength": "3 mg/mL"}], "application_number": "ANDA076513", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20261231"}