ciprofloxacin

Generic: ciprofloxacin

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

Drug Facts

Product Profile

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

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4122
Product ID 68071-4122_1a13ecfc-3490-4377-e063-6394a90ad455
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076639
Listing Expiration 2026-12-31
Marketing Start 2004-09-10

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 680714122
Hyphenated Format 68071-4122

Supplemental Identifiers

RxCUI
309309
UPC
0368071412222
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
  • 10 TABLET in 1 BOTTLE (68071-4122-1)
  • 20 TABLET in 1 BOTTLE (68071-4122-2)
  • 30 TABLET in 1 BOTTLE (68071-4122-3)
  • 14 TABLET in 1 BOTTLE (68071-4122-4)
  • 60 TABLET in 1 BOTTLE (68071-4122-6)
  • 21 TABLET in 1 BOTTLE (68071-4122-7)
source: ndc

Packages (6)

68071-4122-1 10 TABLET in 1 BOTTLE (68071-4122-1) 68071-4122-2 20 TABLET in 1 BOTTLE (68071-4122-2) 68071-4122-3 30 TABLET in 1 BOTTLE (68071-4122-3) 68071-4122-4 14 TABLET in 1 BOTTLE (68071-4122-4) 68071-4122-6 60 TABLET in 1 BOTTLE (68071-4122-6) 68071-4122-7 21 TABLET in 1 BOTTLE (68071-4122-7)

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": "1a13ecfc-3490-4377-e063-6394a90ad455", "openfda": {"upc": ["0368071412222"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["5bab9397-b9f3-d309-e053-2991aa0a6612"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-4122-1)", "package_ndc": "68071-4122-1", "marketing_start_date": "20171016"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4122-2)", "package_ndc": "68071-4122-2", "marketing_start_date": "20171016"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4122-3)", "package_ndc": "68071-4122-3", "marketing_start_date": "20171016"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68071-4122-4)", "package_ndc": "68071-4122-4", "marketing_start_date": "20171016"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-4122-6)", "package_ndc": "68071-4122-6", "marketing_start_date": "20171016"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68071-4122-7)", "package_ndc": "68071-4122-7", "marketing_start_date": "20171016"}], "brand_name": "ciprofloxacin", "product_id": "68071-4122_1a13ecfc-3490-4377-e063-6394a90ad455", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-4122", "generic_name": "ciprofloxacin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}