ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride

Labeler: advagen pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin hydrochloride
Generic Name ciprofloxacin hydrochloride
Labeler advagen pharma limited
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

ciprofloxacin hydrochloride 3 mg/mL

Manufacturer
Advagen Pharma Limited

Identifiers & Regulatory

Product NDC 72888-102
Product ID 72888-102_30142b39-1441-7d9f-e063-6394a90ac169
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075928
Listing Expiration 2026-12-31
Marketing Start 2022-03-16

Pharmacologic Class

Classes
cytochrome p450 1a2 inhibitors [moa] fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72888102
Hyphenated Format 72888-102

Supplemental Identifiers

RxCUI
309307
UPC
0372888102214 0372888102238 0372888102221
UNII
4BA73M5E37

Packaging Origin

Original Packager
true

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 ciprofloxacin hydrochloride (source: ndc)
Generic Name ciprofloxacin hydrochloride (source: ndc)
Application Number ANDA075928 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 3 mg/mL
source: ndc
Packaging
  • 2.5 mL in 1 BOTTLE (72888-102-21)
  • 5 mL in 1 BOTTLE (72888-102-22)
  • 10 mL in 1 BOTTLE (72888-102-23)
source: ndc

Packages (3)

72888-102-21 2.5 mL in 1 BOTTLE (72888-102-21) 72888-102-22 5 mL in 1 BOTTLE (72888-102-22) 72888-102-23 10 mL in 1 BOTTLE (72888-102-23)

Ingredients (1)

ciprofloxacin hydrochloride (3 mg/mL)

Linked Drug Pages (1)

CIPROFLOXACIN HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "30142b39-1441-7d9f-e063-6394a90ac169", "openfda": {"upc": ["0372888102214", "0372888102238", "0372888102221"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["74af98f1-eb6d-473b-94a9-67920dba8c3d"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2.5 mL in 1 BOTTLE (72888-102-21)", "package_ndc": "72888-102-21", "marketing_start_date": "20220316"}, {"sample": false, "description": "5 mL in 1 BOTTLE (72888-102-22)", "package_ndc": "72888-102-22", "marketing_start_date": "20220316"}, {"sample": false, "description": "10 mL in 1 BOTTLE (72888-102-23)", "package_ndc": "72888-102-23", "marketing_start_date": "20220316"}], "brand_name": "CIPROFLOXACIN HYDROCHLORIDE", "product_id": "72888-102_30142b39-1441-7d9f-e063-6394a90ac169", "dosage_form": "SOLUTION", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72888-102", "generic_name": "CIPROFLOXACIN HYDROCHLORIDE", "labeler_name": "Advagen Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPROFLOXACIN HYDROCHLORIDE", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "ANDA075928", "marketing_category": "ANDA", "marketing_start_date": "20220316", "listing_expiration_date": "20261231"}