Package 63323-961-98

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 63323-961-98
Digits Only 6332396198
Product NDC 63323-961
Product ID 63323-961_fd2c8ca9-52d9-4df8-bcd8-8569a4989cd0
Description

1 VIAL in 1 CARTON (63323-961-98) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2014-09-04
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": "fd2c8ca9-52d9-4df8-bcd8-8569a4989cd0", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["f3f9de47-3d85-4d0c-a29e-1635cad3a970"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63323-961-98)  / 5 mL in 1 VIAL", "package_ndc": "63323-961-98", "marketing_start_date": "20140904"}], "brand_name": "Zoledronic Acid", "product_id": "63323-961_fd2c8ca9-52d9-4df8-bcd8-8569a4989cd0", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "63323-961", "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": "4 mg/5mL"}], "application_number": "ANDA202923", "marketing_category": "ANDA", "marketing_start_date": "20140904", "listing_expiration_date": "20261231"}