ciprofloxacin hydrochloride
Generic: ciprofloxacin hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
ciprofloxacin hydrochloride
Generic Name
ciprofloxacin hydrochloride
Labeler
a-s medication solutions
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
ciprofloxacin hydrochloride 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-1754
Product ID
50090-1754_1ba814f1-1d24-423b-b0da-3e9c55834970
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA019992
Listing Expiration
2026-12-31
Marketing Start
2004-05-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500901754
Hyphenated Format
50090-1754
Supplemental Identifiers
RxCUI
UNII
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
NDA019992 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (50090-1754-0) / 2.5 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "1ba814f1-1d24-423b-b0da-3e9c55834970", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["694b79f6-599f-4a71-bf02-d0d09767a735"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50090-1754-0) / 2.5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "50090-1754-0", "marketing_start_date": "20150320"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "50090-1754_1ba814f1-1d24-423b-b0da-3e9c55834970", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-1754", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "NDA019992", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20040507", "listing_expiration_date": "20261231"}