ciprofloxacin

Generic: ciprofolxacin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofolxacin
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4229
Product ID 70518-4229_495de50d-93b8-0884-e063-6294a90a9996
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208921
Listing Expiration 2027-12-31
Marketing Start 2024-11-11

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 705184229
Hyphenated Format 70518-4229

Supplemental Identifiers

RxCUI
309309
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, PLASTIC (70518-4229-0)
  • 20 TABLET in 1 BLISTER PACK (70518-4229-1)
  • 20 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2)
  • 30 TABLET in 1 BLISTER PACK (70518-4229-3)
  • 14 TABLET in 1 BLISTER PACK (70518-4229-4)
  • 14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5)
  • 30 TABLET in 1 BLISTER PACK (70518-4229-6)
  • 30 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7)
source: ndc

Packages (8)

70518-4229-0 14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-0) 70518-4229-1 20 TABLET in 1 BLISTER PACK (70518-4229-1) 70518-4229-2 20 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2) 70518-4229-3 30 TABLET in 1 BLISTER PACK (70518-4229-3) 70518-4229-4 14 TABLET in 1 BLISTER PACK (70518-4229-4) 70518-4229-5 14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5) 70518-4229-6 30 TABLET in 1 BLISTER PACK (70518-4229-6) 70518-4229-7 30 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7)

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": "495de50d-93b8-0884-e063-6294a90a9996", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["c527d138-e32c-418f-9573-a3d8a796279f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-0)", "package_ndc": "70518-4229-0", "marketing_start_date": "20241111"}, {"sample": false, "description": "20 TABLET in 1 BLISTER PACK (70518-4229-1)", "package_ndc": "70518-4229-1", "marketing_start_date": "20241211"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2)", "package_ndc": "70518-4229-2", "marketing_start_date": "20250114"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4229-3)", "package_ndc": "70518-4229-3", "marketing_start_date": "20250129"}, {"sample": false, "description": "14 TABLET in 1 BLISTER PACK (70518-4229-4)", "package_ndc": "70518-4229-4", "marketing_start_date": "20250519"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5)", "package_ndc": "70518-4229-5", "marketing_start_date": "20250709"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4229-6)", "package_ndc": "70518-4229-6", "marketing_start_date": "20250731"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7)", "package_ndc": "70518-4229-7", "marketing_start_date": "20260126"}], "brand_name": "Ciprofloxacin", "product_id": "70518-4229_495de50d-93b8-0884-e063-6294a90a9996", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-4229", "generic_name": "Ciprofolxacin", "labeler_name": "REMEDYREPACK INC.", "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": "20241111", "listing_expiration_date": "20271231"}