Package 68001-611-33

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 68001-611-33
Digits Only 6800161133
Product NDC 68001-611
Description

1 BAG in 1 CARTON (68001-611-33) / 100 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2024-07-06
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": "1f29ce94-b284-836a-e063-6294a90aa50b", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["5de65a7f-a219-4b22-9155-61fedc84433b"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 CARTON (68001-611-33)  / 100 mL in 1 BAG", "package_ndc": "68001-611-33", "marketing_start_date": "20240706"}], "brand_name": "Zoledronic acid", "product_id": "68001-611_1f29ce94-b284-836a-e063-6294a90aa50b", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68001-611", "generic_name": "Zoledronic acid", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA209578", "marketing_category": "ANDA", "marketing_start_date": "20240308", "listing_expiration_date": "20261231"}