cipro hc
Generic: ciprofloxacin hydrochloride and hydrocortisone
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
cipro hc
Generic Name
ciprofloxacin hydrochloride and hydrocortisone
Labeler
asclemed usa, inc.
Dosage Form
SUSPENSION/ DROPS
Routes
Active Ingredients
ciprofloxacin hydrochloride 2 mg/mL, hydrocortisone 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-273
Product ID
76420-273_e80fc4b5-cf91-6430-e053-2995a90a8128
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420273
Hyphenated Format
76420-273
Supplemental Identifiers
RxCUI
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
cipro hc (source: ndc)
Generic Name
ciprofloxacin hydrochloride and hydrocortisone (source: ndc)
Application Number
NDA020805 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
- 10 mg/mL
Packaging
- 10 mL in 1 BOTTLE (76420-273-10)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["AURICULAR (OTIC)"], "spl_id": "e80fc4b5-cf91-6430-e053-2995a90a8128", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["4BA73M5E37", "WI4X0X7BPJ"], "rxcui": ["213320", "309305"], "spl_set_id": ["eafad445-2735-434b-a1c6-e1c6b201d2cf"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE (76420-273-10)", "package_ndc": "76420-273-10", "marketing_start_date": "20220907"}], "brand_name": "CIPRO HC", "product_id": "76420-273_e80fc4b5-cf91-6430-e053-2995a90a8128", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "76420-273", "generic_name": "ciprofloxacin hydrochloride and hydrocortisone", "labeler_name": "Asclemed USA, 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"}