ciprofloxacin

Generic: ciprofloxacin hydrochloride

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

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-997
Product ID 71205-997_1c1b4148-3301-4ab7-8955-667658b4c133
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076126
Listing Expiration 2026-12-31
Marketing Start 2009-10-10

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205997
Hyphenated Format 71205-997

Supplemental Identifiers

RxCUI
309309
UPC
0371205997304
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 hydrochloride (source: ndc)
Application Number ANDA076126 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (71205-997-00)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71205-997-10)
  • 14 TABLET, FILM COATED in 1 BOTTLE (71205-997-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71205-997-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-997-30)
  • 500 TABLET, FILM COATED in 1 BOTTLE (71205-997-55)
source: ndc

Packages (6)

71205-997-00 100 TABLET, FILM COATED in 1 BOTTLE (71205-997-00) 71205-997-10 10 TABLET, FILM COATED in 1 BOTTLE (71205-997-10) 71205-997-14 14 TABLET, FILM COATED in 1 BOTTLE (71205-997-14) 71205-997-20 20 TABLET, FILM COATED in 1 BOTTLE (71205-997-20) 71205-997-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-997-30) 71205-997-55 500 TABLET, FILM COATED in 1 BOTTLE (71205-997-55)

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": "1c1b4148-3301-4ab7-8955-667658b4c133", "openfda": {"upc": ["0371205997304"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["a093ca6e-9963-4eea-b60d-6e2f148192ec"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71205-997-00)", "package_ndc": "71205-997-00", "marketing_start_date": "20200325"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-997-10)", "package_ndc": "71205-997-10", "marketing_start_date": "20200325"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71205-997-14)", "package_ndc": "71205-997-14", "marketing_start_date": "20200325"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-997-20)", "package_ndc": "71205-997-20", "marketing_start_date": "20200325"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-997-30)", "package_ndc": "71205-997-30", "marketing_start_date": "20200325"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71205-997-55)", "package_ndc": "71205-997-55", "marketing_start_date": "20200325"}], "brand_name": "Ciprofloxacin", "product_id": "71205-997_1c1b4148-3301-4ab7-8955-667658b4c133", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "71205-997", "generic_name": "Ciprofloxacin Hydrochloride", "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": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}