Package 72603-198-01

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 72603-198-01
Digits Only 7260319801
Product NDC 72603-198
Description

1 VIAL, GLASS in 1 CARTON (72603-198-01) / 5 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2023-11-01
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": "5499e3f9-5d5d-4eeb-a859-62cc967d468f", "openfda": {"upc": ["0372603198010"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["3885488c-6b83-421b-afee-61abceb95634"], "manufacturer_name": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (72603-198-01)  / 5 mL in 1 VIAL, GLASS", "package_ndc": "72603-198-01", "marketing_start_date": "20231101"}], "brand_name": "Zoledronic acid", "product_id": "72603-198_5499e3f9-5d5d-4eeb-a859-62cc967d468f", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "72603-198", "generic_name": "Zoledronic acid", "labeler_name": "NORTHSTAR RX LLC", "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": "20231101", "listing_expiration_date": "20261231"}