ciprofloxacin

Generic: ciprofloxacin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-017
Product ID 63187-017_91f426fc-3fc4-4c2f-a56d-10862e54d745
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076639
Listing Expiration 2026-12-31
Marketing Start 2004-09-10

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187017
Hyphenated Format 63187-017

Supplemental Identifiers

RxCUI
197511 309309
UPC
0363187142100 0363187017101
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 ANDA076639 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 6 TABLET in 1 BOTTLE (63187-017-06)
  • 10 TABLET in 1 BOTTLE (63187-017-10)
  • 14 TABLET in 1 BOTTLE (63187-017-14)
  • 20 TABLET in 1 BOTTLE (63187-017-20)
  • 28 TABLET in 1 BOTTLE (63187-017-28)
  • 30 TABLET in 1 BOTTLE (63187-017-30)
  • 60 TABLET in 1 BOTTLE (63187-017-60)
  • 90 TABLET in 1 BOTTLE (63187-017-90)
source: ndc

Packages (8)

63187-017-06 6 TABLET in 1 BOTTLE (63187-017-06) 63187-017-10 10 TABLET in 1 BOTTLE (63187-017-10) 63187-017-14 14 TABLET in 1 BOTTLE (63187-017-14) 63187-017-20 20 TABLET in 1 BOTTLE (63187-017-20) 63187-017-28 28 TABLET in 1 BOTTLE (63187-017-28) 63187-017-30 30 TABLET in 1 BOTTLE (63187-017-30) 63187-017-60 60 TABLET in 1 BOTTLE (63187-017-60) 63187-017-90 90 TABLET in 1 BOTTLE (63187-017-90)

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": "91f426fc-3fc4-4c2f-a56d-10862e54d745", "openfda": {"upc": ["0363187142100", "0363187017101"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "309309"], "spl_set_id": ["fbcd32c0-bcfd-4cc7-8e81-6612bc0cfc45"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (63187-017-06)", "package_ndc": "63187-017-06", "marketing_start_date": "20140801"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (63187-017-10)", "package_ndc": "63187-017-10", "marketing_start_date": "20140801"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (63187-017-14)", "package_ndc": "63187-017-14", "marketing_start_date": "20140801"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-017-20)", "package_ndc": "63187-017-20", "marketing_start_date": "20140801"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (63187-017-28)", "package_ndc": "63187-017-28", "marketing_start_date": "20160804"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-017-30)", "package_ndc": "63187-017-30", "marketing_start_date": "20140801"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-017-60)", "package_ndc": "63187-017-60", "marketing_start_date": "20210723"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-017-90)", "package_ndc": "63187-017-90", "marketing_start_date": "20210723"}], "brand_name": "ciprofloxacin", "product_id": "63187-017_91f426fc-3fc4-4c2f-a56d-10862e54d745", "dosage_form": "TABLET", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "63187-017", "generic_name": "ciprofloxacin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}