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 250 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-410
Product ID 43063-410_36b0c0b6-8368-77aa-e063-6394a90a0cc7
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 43063410
Hyphenated Format 43063-410

Supplemental Identifiers

RxCUI
197511
UPC
0343063410202
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
  • 250 mg/1
source: ndc
Packaging
  • 6 TABLET in 1 BOTTLE, PLASTIC (43063-410-06)
  • 10 TABLET in 1 BOTTLE, PLASTIC (43063-410-10)
  • 12 TABLET in 1 BOTTLE, PLASTIC (43063-410-12)
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-410-14)
  • 20 TABLET in 1 BOTTLE, PLASTIC (43063-410-20)
source: ndc

Packages (5)

43063-410-06 6 TABLET in 1 BOTTLE, PLASTIC (43063-410-06) 43063-410-10 10 TABLET in 1 BOTTLE, PLASTIC (43063-410-10) 43063-410-12 12 TABLET in 1 BOTTLE, PLASTIC (43063-410-12) 43063-410-14 14 TABLET in 1 BOTTLE, PLASTIC (43063-410-14) 43063-410-20 20 TABLET in 1 BOTTLE, PLASTIC (43063-410-20)

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": "36b0c0b6-8368-77aa-e063-6394a90a0cc7", "openfda": {"upc": ["0343063410202"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["178dc379-e2b8-4b47-9f0c-3fc7fb435c36"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (43063-410-06)", "package_ndc": "43063-410-06", "marketing_start_date": "20120123"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (43063-410-10)", "package_ndc": "43063-410-10", "marketing_start_date": "20170301"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (43063-410-12)", "package_ndc": "43063-410-12", "marketing_start_date": "20121206"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-410-14)", "package_ndc": "43063-410-14", "marketing_start_date": "20130208"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (43063-410-20)", "package_ndc": "43063-410-20", "marketing_start_date": "20140506"}], "brand_name": "ciprofloxacin", "product_id": "43063-410_36b0c0b6-8368-77aa-e063-6394a90a0cc7", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "43063-410", "generic_name": "ciprofloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}