Package 16252-514-00

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 16252-514-00
Digits Only 1625251400
Product NDC 16252-514
Product ID 16252-514_1f76e627-ddbb-4c59-b9e6-7acb46c0954e
Description

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

Marketing

Marketing Status
Discontinued 2027-08-31
Generic ciprofloxacin

Linked Drug Pages (0)

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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"}