ciprofloxacin

Generic: ciprofloxacin

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-869
Product ID 43063-869_36c1922f-56d3-9a55-e063-6294a90a5571
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 43063869
Hyphenated Format 43063-869

Supplemental Identifiers

RxCUI
309309
UPC
0343063869307
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
  • 6 TABLET in 1 BOTTLE, PLASTIC (43063-869-06)
  • 8 TABLET in 1 BOTTLE, PLASTIC (43063-869-08)
  • 10 TABLET in 1 BOTTLE, PLASTIC (43063-869-10)
  • 20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-869-30)
source: ndc

Packages (5)

43063-869-06 6 TABLET in 1 BOTTLE, PLASTIC (43063-869-06) 43063-869-08 8 TABLET in 1 BOTTLE, PLASTIC (43063-869-08) 43063-869-10 10 TABLET in 1 BOTTLE, PLASTIC (43063-869-10) 43063-869-20 20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20) 43063-869-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-869-30)

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": "36c1922f-56d3-9a55-e063-6294a90a5571", "openfda": {"upc": ["0343063869307"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["e81341c6-0e25-4860-adda-2d3cebe88d62"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (43063-869-06)", "package_ndc": "43063-869-06", "marketing_start_date": "20180804"}, {"sample": false, "description": "8 TABLET in 1 BOTTLE, PLASTIC (43063-869-08)", "package_ndc": "43063-869-08", "marketing_start_date": "20180711"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (43063-869-10)", "package_ndc": "43063-869-10", "marketing_start_date": "20180822"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20)", "package_ndc": "43063-869-20", "marketing_start_date": "20180817"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-869-30)", "package_ndc": "43063-869-30", "marketing_start_date": "20180817"}], "brand_name": "ciprofloxacin", "product_id": "43063-869_36c1922f-56d3-9a55-e063-6294a90a5571", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "43063-869", "generic_name": "ciprofloxacin", "labeler_name": "PD-Rx 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"}