ciprofloxacin hydrochloride
Generic: ciprofloxacin hydrochloride
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
ciprofloxacin hydrochloride
Generic Name
ciprofloxacin hydrochloride
Labeler
nucare pharmaceuticals,inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
ciprofloxacin hydrochloride 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4139
Product ID
68071-4139_2d3feef9-74ea-c651-e063-6394a90a2ca3
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
680714139
Hyphenated Format
68071-4139
Supplemental Identifiers
RxCUI
UPC
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
- 5 mL in 1 BOX (68071-4139-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "2d3feef9-74ea-c651-e063-6394a90a2ca3", "openfda": {"upc": ["0368071413953"], "unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["5cf0f572-48fc-6a3a-e053-2991aa0a8437"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOX (68071-4139-5)", "package_ndc": "68071-4139-5", "marketing_start_date": "20171101"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "68071-4139_2d3feef9-74ea-c651-e063-6394a90a2ca3", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-4139", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}