ciprofloxacin

Generic: ciprofloxacin hydrochloride

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

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4214
Product ID 70518-4214_3ff68934-fd4f-449c-e063-6394a90a465f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077859
Listing Expiration 2026-12-31
Marketing Start 2024-10-15

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 705184214
Hyphenated Format 70518-4214

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 ciprofloxacin hydrochloride (source: ndc)
Application Number ANDA077859 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)
  • 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2)
source: ndc

Packages (3)

70518-4214-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0) 70518-4214-1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1) 70518-4214-2 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2)

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": "3ff68934-fd4f-449c-e063-6394a90a465f", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["47d1e4c5-f669-4aca-9e8c-0d6bb833b859"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0)", "package_ndc": "70518-4214-0", "marketing_start_date": "20241015"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)", "package_ndc": "70518-4214-1", "marketing_start_date": "20241025"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2)", "package_ndc": "70518-4214-2", "marketing_start_date": "20241113"}], "brand_name": "Ciprofloxacin", "product_id": "70518-4214_3ff68934-fd4f-449c-e063-6394a90a465f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-4214", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20241015", "listing_expiration_date": "20261231"}