ciprofloxacin

Generic: ciprofloxacin

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7864
Product ID 68788-7864_77f966b6-f1ac-4e1d-8937-a10f72241d5a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076558
Listing Expiration 2026-12-31
Marketing Start 2021-02-08

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 687887864
Hyphenated Format 68788-7864

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 ANDA076558 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE (68788-7864-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE (68788-7864-1)
  • 20 TABLET, FILM COATED in 1 BOTTLE (68788-7864-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7864-3)
  • 40 TABLET, FILM COATED in 1 BOTTLE (68788-7864-4)
  • 60 TABLET, FILM COATED in 1 BOTTLE, DROPPER (68788-7864-6)
  • 10 TABLET, FILM COATED in 1 BOTTLE (68788-7864-8)
source: ndc

Packages (7)

68788-7864-0 6 TABLET, FILM COATED in 1 BOTTLE (68788-7864-0) 68788-7864-1 14 TABLET, FILM COATED in 1 BOTTLE (68788-7864-1) 68788-7864-2 20 TABLET, FILM COATED in 1 BOTTLE (68788-7864-2) 68788-7864-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7864-3) 68788-7864-4 40 TABLET, FILM COATED in 1 BOTTLE (68788-7864-4) 68788-7864-6 60 TABLET, FILM COATED in 1 BOTTLE, DROPPER (68788-7864-6) 68788-7864-8 10 TABLET, FILM COATED in 1 BOTTLE (68788-7864-8)

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": "77f966b6-f1ac-4e1d-8937-a10f72241d5a", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["f45294bd-e01b-4e21-af82-c788ec73f79a"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68788-7864-0)", "package_ndc": "68788-7864-0", "marketing_start_date": "20210208"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68788-7864-1)", "package_ndc": "68788-7864-1", "marketing_start_date": "20210208"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-7864-2)", "package_ndc": "68788-7864-2", "marketing_start_date": "20210208"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7864-3)", "package_ndc": "68788-7864-3", "marketing_start_date": "20210208"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (68788-7864-4)", "package_ndc": "68788-7864-4", "marketing_start_date": "20210208"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, DROPPER (68788-7864-6)", "package_ndc": "68788-7864-6", "marketing_start_date": "20210208"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68788-7864-8)", "package_ndc": "68788-7864-8", "marketing_start_date": "20210208"}], "brand_name": "Ciprofloxacin", "product_id": "68788-7864_77f966b6-f1ac-4e1d-8937-a10f72241d5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68788-7864", "generic_name": "Ciprofloxacin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20210208", "listing_expiration_date": "20261231"}