cipro hc
Generic: ciprofloxacin hydrochloride and hydrocortisone
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cipro hc
Generic Name
ciprofloxacin hydrochloride and hydrocortisone
Labeler
a-s medication solutions
Dosage Form
SUSPENSION/ DROPS
Routes
Active Ingredients
ciprofloxacin hydrochloride 2 mg/mL, hydrocortisone 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7631
Product ID
50090-7631_76e8bba5-b964-4dbe-a54e-c544db1f3555
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
500907631
Hyphenated Format
50090-7631
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
- 1 BOTTLE in 1 CARTON (50090-7631-0) / 10 mL in 1 BOTTLE
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["AURICULAR (OTIC)"], "spl_id": "76e8bba5-b964-4dbe-a54e-c544db1f3555", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["4BA73M5E37", "WI4X0X7BPJ"], "rxcui": ["213320", "309305"], "spl_set_id": ["d2c40b07-dc39-46c6-8ea1-b288589a46d1"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-7631-0) / 10 mL in 1 BOTTLE", "package_ndc": "50090-7631-0", "marketing_start_date": "20250814"}], "brand_name": "CIPRO HC", "product_id": "50090-7631_76e8bba5-b964-4dbe-a54e-c544db1f3555", "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": "50090-7631", "generic_name": "ciprofloxacin hydrochloride and hydrocortisone", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPRO 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"}