ciprofloxacin

Generic: ciprofloxacin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 750 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-3868
Product ID 63629-3868_8dabad3c-3808-45cc-a58d-127e3a3d6d6b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076558
Listing Expiration 2026-12-31
Marketing Start 2004-06-09

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 636293868
Hyphenated Format 63629-3868

Supplemental Identifiers

RxCUI
197512
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 ANDA076558 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (63629-3868-1)
  • 28 TABLET, FILM COATED in 1 BOTTLE (63629-3868-2)
  • 14 TABLET, FILM COATED in 1 BOTTLE (63629-3868-3)
  • 30 TABLET, FILM COATED in 1 BOTTLE (63629-3868-4)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63629-3868-5)
  • 10 TABLET, FILM COATED in 1 BOTTLE (63629-3868-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7)
source: ndc

Packages (7)

63629-3868-1 20 TABLET, FILM COATED in 1 BOTTLE (63629-3868-1) 63629-3868-2 28 TABLET, FILM COATED in 1 BOTTLE (63629-3868-2) 63629-3868-3 14 TABLET, FILM COATED in 1 BOTTLE (63629-3868-3) 63629-3868-4 30 TABLET, FILM COATED in 1 BOTTLE (63629-3868-4) 63629-3868-5 60 TABLET, FILM COATED in 1 BOTTLE (63629-3868-5) 63629-3868-6 10 TABLET, FILM COATED in 1 BOTTLE (63629-3868-6) 63629-3868-7 90 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7)

Ingredients (1)

ciprofloxacin hydrochloride (750 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": "8dabad3c-3808-45cc-a58d-127e3a3d6d6b", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197512"], "spl_set_id": ["a57066d7-dc2c-d2d0-b003-d9143fcca1c5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (63629-3868-1)", "package_ndc": "63629-3868-1", "marketing_start_date": "20081030"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (63629-3868-2)", "package_ndc": "63629-3868-2", "marketing_start_date": "20090612"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (63629-3868-3)", "package_ndc": "63629-3868-3", "marketing_start_date": "20130423"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-3868-4)", "package_ndc": "63629-3868-4", "marketing_start_date": "20110726"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63629-3868-5)", "package_ndc": "63629-3868-5", "marketing_start_date": "20101214"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (63629-3868-6)", "package_ndc": "63629-3868-6", "marketing_start_date": "20131203"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7)", "package_ndc": "63629-3868-7", "marketing_start_date": "20230306"}], "brand_name": "Ciprofloxacin", "product_id": "63629-3868_8dabad3c-3808-45cc-a58d-127e3a3d6d6b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "63629-3868", "generic_name": "Ciprofloxacin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20040609", "listing_expiration_date": "20261231"}