ciprofloxacin

Generic: ciprofolxacin

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

Drug Facts

Product Profile

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

ciprofloxacin hydrochloride 250 mg/1

Manufacturer
NuCare Pharmaceutical, Inc.

Identifiers & Regulatory

Product NDC 68071-3699
Product ID 68071-3699_4656418d-1f8e-b3bf-e063-6294a90a2401
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208921
Listing Expiration 2026-12-31
Marketing Start 2023-10-01

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 680713699
Hyphenated Format 68071-3699

Supplemental Identifiers

RxCUI
197511
UPC
0368071369939
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 ciprofolxacin (source: ndc)
Application Number ANDA208921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (68071-3699-1)
  • 20 TABLET in 1 BOTTLE (68071-3699-2)
  • 30 TABLET in 1 BOTTLE (68071-3699-3)
  • 6 TABLET in 1 BOTTLE (68071-3699-6)
source: ndc

Packages (4)

68071-3699-1 10 TABLET in 1 BOTTLE (68071-3699-1) 68071-3699-2 20 TABLET in 1 BOTTLE (68071-3699-2) 68071-3699-3 30 TABLET in 1 BOTTLE (68071-3699-3) 68071-3699-6 6 TABLET in 1 BOTTLE (68071-3699-6)

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": "4656418d-1f8e-b3bf-e063-6294a90a2401", "openfda": {"upc": ["0368071369939"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["24760182-4be8-9f43-e063-6294a90a269e"], "manufacturer_name": ["NuCare Pharmaceutical, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-3699-1)", "package_ndc": "68071-3699-1", "marketing_start_date": "20250801"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-3699-2)", "package_ndc": "68071-3699-2", "marketing_start_date": "20251219"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3699-3)", "package_ndc": "68071-3699-3", "marketing_start_date": "20241014"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-3699-6)", "package_ndc": "68071-3699-6", "marketing_start_date": "20241211"}], "brand_name": "Ciprofloxacin", "product_id": "68071-3699_4656418d-1f8e-b3bf-e063-6294a90a2401", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-3699", "generic_name": "Ciprofolxacin", "labeler_name": "NuCare Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}