ciprofloxacin
Generic: ciprofloxacin hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
ciprofloxacin
Generic Name
ciprofloxacin hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ciprofloxacin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-1010
Product ID
63629-1010_fc632cb9-a546-07a9-e053-6394a90a63b9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076126
Listing Expiration
2026-12-31
Marketing Start
2009-10-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636291010
Hyphenated Format
63629-1010
Supplemental Identifiers
RxCUI
UNII
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
ANDA076126 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (63629-1010-1)
- 20 TABLET, FILM COATED in 1 BOTTLE (63629-1010-2)
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-1010-3)
- 14 TABLET, FILM COATED in 1 BOTTLE (63629-1010-4)
- 500 TABLET, FILM COATED in 1 BOTTLE (63629-1010-5)
- 60 TABLET, FILM COATED in 1 BOTTLE (63629-1010-6)
- 10 TABLET, FILM COATED in 1 BOTTLE (63629-1010-7)
- 120 TABLET, FILM COATED in 1 BOTTLE (63629-1010-8)
Packages (8)
63629-1010-1
100 TABLET, FILM COATED in 1 BOTTLE (63629-1010-1)
63629-1010-2
20 TABLET, FILM COATED in 1 BOTTLE (63629-1010-2)
63629-1010-3
30 TABLET, FILM COATED in 1 BOTTLE (63629-1010-3)
63629-1010-4
14 TABLET, FILM COATED in 1 BOTTLE (63629-1010-4)
63629-1010-5
500 TABLET, FILM COATED in 1 BOTTLE (63629-1010-5)
63629-1010-6
60 TABLET, FILM COATED in 1 BOTTLE (63629-1010-6)
63629-1010-7
10 TABLET, FILM COATED in 1 BOTTLE (63629-1010-7)
63629-1010-8
120 TABLET, FILM COATED in 1 BOTTLE (63629-1010-8)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc632cb9-a546-07a9-e053-6394a90a63b9", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["8eef4f14-e7ef-41be-be57-7993b333e8a9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (63629-1010-1)", "package_ndc": "63629-1010-1", "marketing_start_date": "20201207"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (63629-1010-2)", "package_ndc": "63629-1010-2", "marketing_start_date": "20200923"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-1010-3)", "package_ndc": "63629-1010-3", "marketing_start_date": "20220406"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (63629-1010-4)", "package_ndc": "63629-1010-4", "marketing_start_date": "20211025"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63629-1010-5)", "package_ndc": "63629-1010-5", "marketing_start_date": "20201117"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63629-1010-6)", "package_ndc": "63629-1010-6", "marketing_start_date": "20220406"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (63629-1010-7)", "package_ndc": "63629-1010-7", "marketing_start_date": "20220406"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (63629-1010-8)", "package_ndc": "63629-1010-8", "marketing_start_date": "20220406"}], "brand_name": "Ciprofloxacin", "product_id": "63629-1010_fc632cb9-a546-07a9-e053-6394a90a63b9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "63629-1010", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}