ciprofloxacin

Generic: ciprofloxacin

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler sagent pharmaceuticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ciprofloxacin 2 mg/mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-114
Product ID 25021-114_c30953aa-a1e5-45b5-97a5-6bb9d0b0bd6f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078252
Listing Expiration 2026-12-31
Marketing Start 2008-03-24

Pharmacologic Class

Established (EPC)
fluoroquinolone antibacterial [epc]
Mechanism of Action
cytochrome p450 1a2 inhibitors [moa]
Chemical Structure
fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021114
Hyphenated Format 25021-114

Supplemental Identifiers

RxCUI
1665210 1665212
UNII
5E8K9I0O4U
NUI
N0000193223 M0372253 N0000182138

Packaging Origin

Original Packager
true

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 ANDA078252 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 24 POUCH in 1 CARTON (25021-114-82) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
  • 24 POUCH in 1 CARTON (25021-114-87) / 1 BAG in 1 POUCH / 200 mL in 1 BAG
source: ndc

Packages (2)

25021-114-82 24 POUCH in 1 CARTON (25021-114-82) / 1 BAG in 1 POUCH / 100 mL in 1 BAG 25021-114-87 24 POUCH in 1 CARTON (25021-114-87) / 1 BAG in 1 POUCH / 200 mL in 1 BAG

Ingredients (1)

ciprofloxacin (2 mg/mL)

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c30953aa-a1e5-45b5-97a5-6bb9d0b0bd6f", "openfda": {"nui": ["N0000193223", "M0372253", "N0000182138"], "unii": ["5E8K9I0O4U"], "rxcui": ["1665210", "1665212"], "spl_set_id": ["7049f870-6741-4a67-8033-398c36126a06"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "pharm_class_moa": ["Cytochrome P450 1A2 Inhibitors [MoA]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CARTON (25021-114-82)  / 1 BAG in 1 POUCH / 100 mL in 1 BAG", "package_ndc": "25021-114-82", "marketing_start_date": "20080324"}, {"sample": false, "description": "24 POUCH in 1 CARTON (25021-114-87)  / 1 BAG in 1 POUCH / 200 mL in 1 BAG", "package_ndc": "25021-114-87", "marketing_start_date": "20080324"}], "brand_name": "Ciprofloxacin", "product_id": "25021-114_c30953aa-a1e5-45b5-97a5-6bb9d0b0bd6f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "25021-114", "generic_name": "ciprofloxacin", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN", "strength": "2 mg/mL"}], "application_number": "ANDA078252", "marketing_category": "ANDA", "marketing_start_date": "20080324", "listing_expiration_date": "20261231"}