ofloxacin

Generic: ofloxacin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ofloxacin
Generic Name ofloxacin
Labeler proficient rx lp
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

ofloxacin 3 mg/mL

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-420
Product ID 71205-420_e65f9309-c5da-4159-ba09-28754fe12593
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)
quinolone antimicrobial [epc]
Chemical Structure
quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205420
Hyphenated Format 71205-420

Supplemental Identifiers

RxCUI
312075
UPC
0371205420055
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 ANDA076513 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 3 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (71205-420-05) / 5 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

71205-420-05 1 BOTTLE, DROPPER in 1 CARTON (71205-420-05) / 5 mL in 1 BOTTLE, DROPPER

Ingredients (1)

ofloxacin (3 mg/mL)

Linked Drug Pages (1)

Ofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "e65f9309-c5da-4159-ba09-28754fe12593", "openfda": {"nui": ["N0000175937", "M0023650"], "upc": ["0371205420055"], "unii": ["A4P49JAZ9H"], "rxcui": ["312075"], "spl_set_id": ["5a9de529-6f85-467a-97b0-8ce124c31173"], "pharm_class_cs": ["Quinolones [CS]"], "pharm_class_epc": ["Quinolone Antimicrobial [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (71205-420-05)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "71205-420-05", "marketing_start_date": "20200301"}], "brand_name": "Ofloxacin", "product_id": "71205-420_e65f9309-c5da-4159-ba09-28754fe12593", "dosage_form": "SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71205-420", "generic_name": "ofloxacin", "labeler_name": "Proficient Rx LP", "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"}