Package 68001-437-25

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 68001-437-25
Digits Only 6800143725
Product NDC 68001-437
Product ID 68001-437_0179cc91-4a11-1cc0-e063-6294a90a6c1e
Description

1 VIAL in 1 CARTON (68001-437-25) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-06-29
Brand zoledronic acid
Generic zoledronic acid
Sample Package No

Linked Drug Pages (1)

Zoledronic acid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0179cc91-4a11-1cc0-e063-6294a90a6c1e", "openfda": {"upc": ["0368001437257"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["666b1833-ee9b-4a6f-bd4c-9526552cec0a"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-437-25)  / 5 mL in 1 VIAL", "package_ndc": "68001-437-25", "marketing_start_date": "20200629"}], "brand_name": "Zoledronic acid", "product_id": "68001-437_0179cc91-4a11-1cc0-e063-6294a90a6c1e", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68001-437", "generic_name": "zoledronic acid", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA205279", "marketing_category": "ANDA", "marketing_start_date": "20200629", "listing_expiration_date": "20261231"}