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
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-623
Product ID 72189-623_4c9a9248-b591-7e0a-e063-6394a90a884d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208921
Listing Expiration 2027-12-31
Marketing Start 2025-05-14

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 72189623
Hyphenated Format 72189-623

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 ANDA208921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (72189-623-10)
  • 14 TABLET in 1 BOTTLE (72189-623-14)
  • 20 TABLET in 1 BOTTLE (72189-623-20)
source: ndc

Packages (3)

72189-623-10 10 TABLET in 1 BOTTLE (72189-623-10) 72189-623-14 14 TABLET in 1 BOTTLE (72189-623-14) 72189-623-20 20 TABLET in 1 BOTTLE (72189-623-20)

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": "4c9a9248-b591-7e0a-e063-6394a90a884d", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["351b41db-622f-a1eb-e063-6294a90a5667"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (72189-623-10)", "package_ndc": "72189-623-10", "marketing_start_date": "20250514"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (72189-623-14)", "package_ndc": "72189-623-14", "marketing_start_date": "20250514"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-623-20)", "package_ndc": "72189-623-20", "marketing_start_date": "20250514"}], "brand_name": "Ciprofloxacin", "product_id": "72189-623_4c9a9248-b591-7e0a-e063-6394a90a884d", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72189-623", "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": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20250514", "listing_expiration_date": "20271231"}