Package 67457-619-10

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 67457-619-10
Digits Only 6745761910
Product NDC 67457-619
Description

1 VIAL in 1 CARTON (67457-619-10) / 100 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-05-19
Brand zoledronic acid
Generic zoledronic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f90dcc52-1a24-4e7f-88a8-851e70b90250", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["1977d713-4cc7-405e-b4c1-a9a91635eff6"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (67457-619-10)  / 100 mL in 1 VIAL", "package_ndc": "67457-619-10", "marketing_start_date": "20170519"}], "brand_name": "Zoledronic Acid", "product_id": "67457-619_f90dcc52-1a24-4e7f-88a8-851e70b90250", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "67457-619", "generic_name": "Zoledronic Acid", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA203841", "marketing_category": "ANDA", "marketing_start_date": "20170519", "listing_expiration_date": "20271231"}