ciprofloxacin

Generic: ciprofloxacin

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 750 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 16252-516
Product ID 16252-516_102b18ad-5814-4bda-9b89-2991af2480e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076794
Marketing Start 2006-11-01
Marketing End 2026-03-31

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 16252516
Hyphenated Format 16252-516

Supplemental Identifiers

RxCUI
197511 197512 309309
UPC
0316252515019
UNII
4BA73M5E37

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 ANDA076794 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-516-05)
source: ndc

Packages (1)

16252-516-05 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-516-05)

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": "102b18ad-5814-4bda-9b89-2991af2480e1", "openfda": {"upc": ["0316252515019"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["3e4402d4-e0d3-9846-3e81-ed46f34137fe"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-516-05)", "package_ndc": "16252-516-05", "marketing_end_date": "20260331", "marketing_start_date": "20061101"}], "brand_name": "Ciprofloxacin", "product_id": "16252-516_102b18ad-5814-4bda-9b89-2991af2480e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "16252-516", "generic_name": "Ciprofloxacin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076794", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20061101"}