Package 71288-806-51

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 71288-806-51
Digits Only 7128880651
Product NDC 71288-806
Description

1 BOTTLE, GLASS in 1 CARTON (71288-806-51) / 100 mL in 1 BOTTLE, GLASS

Marketing

Marketing Status
Marketed Since 2023-06-05
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": "a4589df5-8c10-4040-ba54-637c518a0e11", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["8aac81ae-f92c-4f0b-b480-44badf72b5f5"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (71288-806-51)  / 100 mL in 1 BOTTLE, GLASS", "package_ndc": "71288-806-51", "marketing_start_date": "20230605"}], "brand_name": "Zoledronic Acid", "product_id": "71288-806_a4589df5-8c10-4040-ba54-637c518a0e11", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "71288-806", "generic_name": "Zoledronic Acid", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA213371", "marketing_category": "ANDA", "marketing_start_date": "20230605", "listing_expiration_date": "20261231"}