ciprofloxacin

Generic: ciprofloxacin

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-627
Product ID 72189-627_49780801-4d94-7029-e063-6294a90a28b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077859
Marketing Start 2025-06-05
Marketing End 2028-02-29

Pharmacologic Class

Classes
cytochrome p450 1a2 inhibitors [moa] fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189627
Hyphenated Format 72189-627

Supplemental Identifiers

RxCUI
309309
UNII
4BA73M5E37

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 (source: ndc)
Application Number ANDA077859 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (72189-627-10)
  • 14 TABLET, FILM COATED in 1 BOTTLE (72189-627-14)
source: ndc

Packages (2)

72189-627-10 10 TABLET, FILM COATED in 1 BOTTLE (72189-627-10) 72189-627-14 14 TABLET, FILM COATED in 1 BOTTLE (72189-627-14)

Ingredients (1)

ciprofloxacin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49780801-4d94-7029-e063-6294a90a28b7", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["36d6c27d-45dc-3081-e063-6394a90a87e9"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (72189-627-10)", "package_ndc": "72189-627-10", "marketing_end_date": "20280229", "marketing_start_date": "20250605"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (72189-627-14)", "package_ndc": "72189-627-14", "marketing_end_date": "20280229", "marketing_start_date": "20250605"}], "brand_name": "Ciprofloxacin", "product_id": "72189-627_49780801-4d94-7029-e063-6294a90a28b7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-627", "generic_name": "Ciprofloxacin", "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": "20280229", "marketing_start_date": "20250605"}