Package 68083-142-01

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 68083-142-01
Digits Only 6808314201
Product NDC 68083-142
Description

1 VIAL in 1 CARTON (68083-142-01) / 100 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-07-05
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": "a1d17413-5a66-4bc0-8369-c91d360bc2a8", "openfda": {"upc": ["0368083142018"], "unii": ["6XC1PAD3KF"], "rxcui": ["1114085"], "spl_set_id": ["1740d7d8-a101-4688-8d8b-beb00559d602"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68083-142-01)  / 100 mL in 1 VIAL", "package_ndc": "68083-142-01", "marketing_start_date": "20180705"}], "brand_name": "Zoledronic Acid", "product_id": "68083-142_a1d17413-5a66-4bc0-8369-c91d360bc2a8", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68083-142", "generic_name": "zoledronic Acid", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/100mL"}], "application_number": "ANDA205749", "marketing_category": "ANDA", "marketing_start_date": "20180705", "listing_expiration_date": "20261231"}