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, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2267
Product ID 68071-2267_1d76786e-4b8e-9489-e063-6294a90a2a17
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076794
Listing Expiration 2026-12-31
Marketing Start 2006-11-01

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 680712267
Hyphenated Format 68071-2267

Supplemental Identifiers

RxCUI
309309
UPC
0368071226713
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 ANDA076794 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)
source: ndc

Packages (1)

68071-2267-1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)

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": "1d76786e-4b8e-9489-e063-6294a90a2a17", "openfda": {"upc": ["0368071226713"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["b0136d72-0869-2da0-e053-2995a90af70a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)", "package_ndc": "68071-2267-1", "marketing_start_date": "20200924"}], "brand_name": "Ciprofloxacin", "product_id": "68071-2267_1d76786e-4b8e-9489-e063-6294a90a2a17", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-2267", "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": "ANDA076794", "marketing_category": "ANDA", "marketing_start_date": "20061101", "listing_expiration_date": "20261231"}