cipro hc

Generic: ciprofloxacin hydrochloride and hydrocortisone

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cipro hc
Generic Name ciprofloxacin hydrochloride and hydrocortisone
Labeler sandoz inc
Dosage Form SUSPENSION/ DROPS
Routes
AURICULAR (OTIC)
Active Ingredients

ciprofloxacin hydrochloride 2 mg/mL, hydrocortisone 10 mg/mL

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 66758-087
Product ID 66758-087_7c5775a8-2754-4652-b57a-75bbf32dfbe6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020805
Listing Expiration 2026-12-31
Marketing Start 1999-03-15

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66758087
Hyphenated Format 66758-087

Supplemental Identifiers

RxCUI
213320 309305
UNII
4BA73M5E37 WI4X0X7BPJ
NUI
N0000175576 N0000175450

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 cipro hc (source: ndc)
Generic Name ciprofloxacin hydrochloride and hydrocortisone (source: ndc)
Application Number NDA020805 (source: ndc)
Routes
AURICULAR (OTIC)
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
  • 10 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (66758-087-70) / 10 mL in 1 BOTTLE
source: ndc

Packages (1)

66758-087-70 1 BOTTLE in 1 CARTON (66758-087-70) / 10 mL in 1 BOTTLE

Ingredients (2)

ciprofloxacin hydrochloride (2 mg/mL) hydrocortisone (10 mg/mL)

Linked Drug Pages (1)

CIPRO HC ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["AURICULAR (OTIC)"], "spl_id": "7c5775a8-2754-4652-b57a-75bbf32dfbe6", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["4BA73M5E37", "WI4X0X7BPJ"], "rxcui": ["213320", "309305"], "spl_set_id": ["b26594a3-2adf-4954-8be0-5bd6f8de9671"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (66758-087-70)  / 10 mL in 1 BOTTLE", "package_ndc": "66758-087-70", "marketing_start_date": "20241108"}], "brand_name": "CIPRO HC", "product_id": "66758-087_7c5775a8-2754-4652-b57a-75bbf32dfbe6", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "66758-087", "generic_name": "ciprofloxacin hydrochloride and hydrocortisone", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPRO", "brand_name_suffix": "HC", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "2 mg/mL"}, {"name": "HYDROCORTISONE", "strength": "10 mg/mL"}], "application_number": "NDA020805", "marketing_category": "NDA", "marketing_start_date": "19990315", "listing_expiration_date": "20261231"}