ciprofloxacin

Generic: ciprofolxacin

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofolxacin
Labeler redpharm drug
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2135
Product ID 67296-2135_46aca6ab-7485-ab8c-e063-6394a90a3aa6
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 672962135
Hyphenated Format 67296-2135

Supplemental Identifiers

RxCUI
309309
UPC
0343547689100 0343547688103
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
  • 500 mg/1
source: ndc
Packaging
  • 14 TABLET in 1 BOTTLE (67296-2135-1)
  • 10 TABLET in 1 BOTTLE (67296-2135-2)
  • 20 TABLET in 1 BOTTLE (67296-2135-3)
  • 6 TABLET in 1 BOTTLE (67296-2135-6)
source: ndc

Packages (4)

67296-2135-1 14 TABLET in 1 BOTTLE (67296-2135-1) 67296-2135-2 10 TABLET in 1 BOTTLE (67296-2135-2) 67296-2135-3 20 TABLET in 1 BOTTLE (67296-2135-3) 67296-2135-6 6 TABLET in 1 BOTTLE (67296-2135-6)

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": "46aca6ab-7485-ab8c-e063-6394a90a3aa6", "openfda": {"upc": ["0343547689100", "0343547688103"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["3253a41f-4f0a-5d83-e063-6294a90a890c"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (67296-2135-1)", "package_ndc": "67296-2135-1", "marketing_start_date": "20231001"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (67296-2135-2)", "package_ndc": "67296-2135-2", "marketing_start_date": "20231001"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (67296-2135-3)", "package_ndc": "67296-2135-3", "marketing_start_date": "20231001"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (67296-2135-6)", "package_ndc": "67296-2135-6", "marketing_start_date": "20231001"}], "brand_name": "Ciprofloxacin", "product_id": "67296-2135_46aca6ab-7485-ab8c-e063-6394a90a3aa6", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "67296-2135", "generic_name": "Ciprofolxacin", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}