Package 68083-135-01

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 68083-135-01
Digits Only 6808313501
Product NDC 68083-135
Product ID 68083-135_d6e2e420-9322-4f59-9856-05104642fbc2
Description

1 VIAL, GLASS in 1 CARTON (68083-135-01) / 100 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2016-09-15
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": "d6e2e420-9322-4f59-9856-05104642fbc2", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["824eaeee-6b3d-4d62-b268-77f8bd8e7f10"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (68083-135-01)  / 100 mL in 1 VIAL, GLASS", "package_ndc": "68083-135-01", "marketing_start_date": "20160915"}], "brand_name": "Zoledronic Acid", "product_id": "68083-135_d6e2e420-9322-4f59-9856-05104642fbc2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68083-135", "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": "5 mg/100mL"}], "application_number": "ANDA204217", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20271231"}