ciprofloxacin

Generic: ciprofloxacin

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

ciprofloxacin hydrochloride 250 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-214
Product ID 76420-214_d9b54ffb-864f-1ca8-e053-2995a90a5144
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076558
Listing Expiration 2026-12-31
Marketing Start 2004-06-09

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420214
Hyphenated Format 76420-214

Supplemental Identifiers

RxCUI
197511
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
  • 250 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE (76420-214-06)
  • 10 TABLET, FILM COATED in 1 BOTTLE (76420-214-10)
  • 14 TABLET, FILM COATED in 1 BOTTLE (76420-214-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (76420-214-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (76420-214-30)
source: ndc

Packages (5)

76420-214-06 6 TABLET, FILM COATED in 1 BOTTLE (76420-214-06) 76420-214-10 10 TABLET, FILM COATED in 1 BOTTLE (76420-214-10) 76420-214-14 14 TABLET, FILM COATED in 1 BOTTLE (76420-214-14) 76420-214-20 20 TABLET, FILM COATED in 1 BOTTLE (76420-214-20) 76420-214-30 30 TABLET, FILM COATED in 1 BOTTLE (76420-214-30)

Ingredients (1)

ciprofloxacin hydrochloride (250 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": "d9b54ffb-864f-1ca8-e053-2995a90a5144", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["1bb1d26e-fad0-4338-8948-3f095d5817a6"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (76420-214-06)", "package_ndc": "76420-214-06", "marketing_start_date": "20220308"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (76420-214-10)", "package_ndc": "76420-214-10", "marketing_start_date": "20220308"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (76420-214-14)", "package_ndc": "76420-214-14", "marketing_start_date": "20220308"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (76420-214-20)", "package_ndc": "76420-214-20", "marketing_start_date": "20220308"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-214-30)", "package_ndc": "76420-214-30", "marketing_start_date": "20220308"}], "brand_name": "Ciprofloxacin", "product_id": "76420-214_d9b54ffb-864f-1ca8-e053-2995a90a5144", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "76420-214", "generic_name": "Ciprofloxacin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20040609", "listing_expiration_date": "20261231"}