Package 69367-190-50

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 69367-190-50
Digits Only 6936719050
Product NDC 69367-190
Product ID 69367-190_d8c7e44e-b472-4c33-bfd7-1eb9d18b4a0f
Description

1 VIAL in 1 CARTON (69367-190-50) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-02-02
Brand zoledronic acid
Generic zoledronic acid
Sample Package No

Linked Drug Pages (1)

Zoledronic Acid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "d8c7e44e-b472-4c33-bfd7-1eb9d18b4a0f", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["6a153c94-3cb5-4c05-98b2-1e18f5f3fe80"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (69367-190-50)  / 5 mL in 1 VIAL", "package_ndc": "69367-190-50", "marketing_start_date": "20230202"}], "brand_name": "Zoledronic Acid", "product_id": "69367-190_d8c7e44e-b472-4c33-bfd7-1eb9d18b4a0f", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "69367-190", "generic_name": "Zoledronic Acid", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA202923", "marketing_category": "ANDA", "marketing_start_date": "20230202", "listing_expiration_date": "20261231"}