ciprofloxacin

Generic: ciprofloxacin hydrochloride

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler golden state medical supply, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 51407-165
Product ID 51407-165_2ee94e9b-43b8-e3d5-e063-6394a90ae89b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076126
Listing Expiration 2026-12-31
Marketing Start 2004-06-09

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 51407165
Hyphenated Format 51407-165

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 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 (51407-165-01)
  • 20 TABLET, FILM COATED in 1 BOTTLE (51407-165-20)
  • 28 TABLET, FILM COATED in 1 BOTTLE (51407-165-28)
source: ndc

Packages (3)

51407-165-01 100 TABLET, FILM COATED in 1 BOTTLE (51407-165-01) 51407-165-20 20 TABLET, FILM COATED in 1 BOTTLE (51407-165-20) 51407-165-28 28 TABLET, FILM COATED in 1 BOTTLE (51407-165-28)

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": "2ee94e9b-43b8-e3d5-e063-6394a90ae89b", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["d17b0e87-b555-4dfb-e053-2a95a90aa5ef"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51407-165-01)", "package_ndc": "51407-165-01", "marketing_start_date": "20211005"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (51407-165-20)", "package_ndc": "51407-165-20", "marketing_start_date": "20230206"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (51407-165-28)", "package_ndc": "51407-165-28", "marketing_start_date": "20240124"}], "brand_name": "Ciprofloxacin", "product_id": "51407-165_2ee94e9b-43b8-e3d5-e063-6394a90ae89b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "51407-165", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "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": "20040609", "listing_expiration_date": "20261231"}