ciprofloxacin
Generic: ciprofloxacin hydrochloride
Labeler: direct rxDrug Facts
Product Profile
Brand Name
ciprofloxacin
Generic Name
ciprofloxacin hydrochloride
Labeler
direct rx
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ciprofloxacin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-111
Product ID
72189-111_4c499af5-b74b-2799-e063-6294a90a7054
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077859
Marketing Start
2020-06-12
Marketing End
2027-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189111
Hyphenated Format
72189-111
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 (source: ndc)
Generic Name
ciprofloxacin hydrochloride (source: ndc)
Application Number
ANDA077859 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 10 TABLET, FILM COATED in 1 BOTTLE (72189-111-10)
- 14 TABLET, FILM COATED in 1 BOTTLE (72189-111-14)
- 20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c499af5-b74b-2799-e063-6294a90a7054", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["a7e5174a-dd01-6050-e053-2a95a90add3f"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (72189-111-10)", "package_ndc": "72189-111-10", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (72189-111-14)", "package_ndc": "72189-111-14", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)", "package_ndc": "72189-111-20", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)", "package_ndc": "72189-111-30", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}], "brand_name": "CIPROFLOXACIN", "product_id": "72189-111_4c499af5-b74b-2799-e063-6294a90a7054", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-111", "generic_name": "ciprofloxacin hydrochloride", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIPROFLOXACIN", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20270228", "marketing_start_date": "20200612"}