Package 63323-966-00

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 63323-966-00
Digits Only 6332396600
Product NDC 63323-966
Product ID 63323-966_9fb5ae91-44b4-4b48-aaeb-0a2ba676aa16
Description

1 VIAL, GLASS in 1 CARTON (63323-966-00) / 100 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2017-02-17
Brand zoledronic acid
Generic zoledronic acid
Sample Package No

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "9fb5ae91-44b4-4b48-aaeb-0a2ba676aa16", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["16fcf8c9-ef8a-4e93-9ee6-acfadd35a861"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (63323-966-00)  / 100 mL in 1 VIAL, GLASS", "package_ndc": "63323-966-00", "marketing_start_date": "20170217"}], "brand_name": "Zoledronic Acid", "product_id": "63323-966_9fb5ae91-44b4-4b48-aaeb-0a2ba676aa16", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "63323-966", "generic_name": "Zoledronic Acid", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA204217", "marketing_category": "ANDA", "marketing_start_date": "20170217", "listing_expiration_date": "20261231"}