16252-514

Generic: ciprofloxacin

Labeler: teva pharmaceuticals usa, inc.
NDC Directory DRUG FOR FURTHER PROCESSING DRUG FOR FURTHER PROCESSING Active

Drug Facts

Product Profile

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

ciprofloxacin hydrochloride 250 mg/1

Identifiers & Regulatory

Product NDC 16252-514
Product ID 16252-514_1f76e627-ddbb-4c59-b9e6-7acb46c0954e
Product Type DRUG FOR FURTHER PROCESSING
Marketing Category DRUG FOR FURTHER PROCESSING
Marketing Start 2004-06-09
Marketing End 2027-08-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16252514
Hyphenated Format 16252-514

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: label)
Generic Name ciprofloxacin (source: ndc)
Application Number ANDA076794 (source: label)
Routes
oral
source: label

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 24630 TABLET, FILM COATED in 1 BOX (16252-514-00)
source: ndc

Packages (1)

16252-514-00 24630 TABLET, FILM COATED in 1 BOX (16252-514-00)

Ingredients (1)

ciprofloxacin hydrochloride (250 mg/1)

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "1f76e627-ddbb-4c59-b9e6-7acb46c0954e", "openfda": {}, "finished": false, "packaging": [{"description": "24630 TABLET, FILM COATED in 1 BOX (16252-514-00)", "package_ndc": "16252-514-00", "marketing_end_date": "31-AUG-27", "marketing_start_date": "09-JUN-04"}], "product_id": "16252-514_1f76e627-ddbb-4c59-b9e6-7acb46c0954e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "16252-514", "generic_name": "Ciprofloxacin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_end_date": "20270831", "marketing_start_date": "20040609"}