ciprofloxacin hydrochloride
Generic: ciprofloxacin hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
ciprofloxacin hydrochloride
Generic Name
ciprofloxacin hydrochloride
Labeler
remedyrepack inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
ciprofloxacin hydrochloride 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1170
Product ID
70518-1170_36e8be23-f959-0d00-e063-6294a90ae770
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA019992
Listing Expiration
2026-12-31
Marketing Start
2018-05-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181170
Hyphenated Format
70518-1170
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 (70518-1170-0) / 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": "36e8be23-f959-0d00-e063-6294a90ae770", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["a2cec2cc-729b-4baa-8df1-c3f70847a483"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70518-1170-0) / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "70518-1170-0", "marketing_start_date": "20180515"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "70518-1170_36e8be23-f959-0d00-e063-6294a90ae770", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-1170", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "REMEDYREPACK 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": "20180515", "listing_expiration_date": "20261231"}