Package 55150-266-05

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 55150-266-05
Digits Only 5515026605
Product NDC 55150-266
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (55150-266-05) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2016-09-26
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": "c85e7c96-b74d-41ee-a07a-c3bc44ca4fc8", "openfda": {"upc": ["0355150266050"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["ac7ff1eb-6e73-4cc8-9114-c5a4483ad4c3"], "manufacturer_name": ["AuroMedics Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (55150-266-05)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-266-05", "marketing_start_date": "20160926"}], "brand_name": "Zoledronic Acid", "product_id": "55150-266_c85e7c96-b74d-41ee-a07a-c3bc44ca4fc8", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "55150-266", "generic_name": "Zoledronic Acid", "labeler_name": "AuroMedics Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA207751", "marketing_category": "ANDA", "marketing_start_date": "20160926", "listing_expiration_date": "20261231"}