Package 23155-170-31

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 23155-170-31
Digits Only 2315517031
Product NDC 23155-170
Description

1 VIAL, GLASS in 1 CARTON (23155-170-31) / 5 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2023-08-31
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": "f4991976-8a87-4a00-839f-3f62c561c230", "openfda": {"upc": ["0323155170313"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["00a5bd5a-e5ee-4bad-b510-a4d4485485c8"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (23155-170-31)  / 5 mL in 1 VIAL, GLASS", "package_ndc": "23155-170-31", "marketing_start_date": "20230831"}], "brand_name": "Zoledronic acid", "product_id": "23155-170_f4991976-8a87-4a00-839f-3f62c561c230", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "23155-170", "generic_name": "Zoledronic acid", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA201783", "marketing_category": "ANDA", "marketing_start_date": "20230831", "listing_expiration_date": "20261231"}