ofloxacin

Generic: ofloxacin

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ofloxacin
Generic Name ofloxacin
Labeler nucare pharmaceuticals, inc.
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

ofloxacin 3 mg/mL

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-1607
Product ID 68071-1607_2a07b00e-964b-c66b-e063-6394a90a4822
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076407
Listing Expiration 2026-12-31
Marketing Start 2008-07-01

Pharmacologic Class

Established (EPC)
quinolone antimicrobial [epc]
Chemical Structure
quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680711607
Hyphenated Format 68071-1607

Supplemental Identifiers

RxCUI
312075
UPC
0368071160758
UNII
A4P49JAZ9H
NUI
N0000175937 M0023650

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 ANDA076407 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 3 mg/mL
source: ndc
Packaging
  • 5 mL in 1 BOX (68071-1607-5)
source: ndc

Packages (1)

Ingredients (1)

ofloxacin (3 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "2a07b00e-964b-c66b-e063-6394a90a4822", "openfda": {"nui": ["N0000175937", "M0023650"], "upc": ["0368071160758"], "unii": ["A4P49JAZ9H"], "rxcui": ["312075"], "spl_set_id": ["51f3d155-36df-4c40-e054-00144ff8d46c"], "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 BOX (68071-1607-5)", "package_ndc": "68071-1607-5", "marketing_start_date": "20170614"}], "brand_name": "Ofloxacin", "product_id": "68071-1607_2a07b00e-964b-c66b-e063-6394a90a4822", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "68071-1607", "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": "ANDA076407", "marketing_category": "ANDA", "marketing_start_date": "20080701", "listing_expiration_date": "20261231"}