Package 68083-116-01

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 68083-116-01
Digits Only 6808311601
Product NDC 68083-116
Description

1 VIAL in 1 CARTON (68083-116-01) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2013-09-20
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": "c08f4eee-1566-4493-83f7-48fa1319a234", "openfda": {"upc": ["0368083615017", "0368083116019"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["7a5e8962-7c4b-40bb-ad69-0c3edb0338af"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68083-116-01)  / 5 mL in 1 VIAL", "package_ndc": "68083-116-01", "marketing_start_date": "20130920"}], "brand_name": "Zoledronic Acid", "product_id": "68083-116_c08f4eee-1566-4493-83f7-48fa1319a234", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68083-116", "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/5mL"}], "application_number": "ANDA202930", "marketing_category": "ANDA", "marketing_start_date": "20130920", "listing_expiration_date": "20261231"}