Package 55111-685-07

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 55111-685-07
Digits Only 5511168507
Product NDC 55111-685
Description

1 VIAL, GLASS in 1 CARTON (55111-685-07) / 5 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2013-03-04
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": "f524daa0-1742-f647-b08e-46a0477c1540", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["1738a682-5903-b675-3a7a-61d299a6f248"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (55111-685-07)  / 5 mL in 1 VIAL, GLASS", "package_ndc": "55111-685-07", "marketing_start_date": "20130304"}], "brand_name": "Zoledronic Acid", "product_id": "55111-685_f524daa0-1742-f647-b08e-46a0477c1540", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "55111-685", "generic_name": "Zoledronic Acid", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA091186", "marketing_category": "ANDA", "marketing_start_date": "20130304", "listing_expiration_date": "20261231"}