Package 55111-688-52

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 55111-688-52
Digits Only 5511168852
Product NDC 55111-688
Description

100 mL in 1 BOTTLE, GLASS (55111-688-52)

Marketing

Marketing Status
Marketed Since 2013-04-03
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": "251add88-5c4f-2750-c713-744fcf3a60ba", "openfda": {"upc": ["0355111688525"], "unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["f94a5c9e-74bc-d09e-cd65-394b2a5de2ad"], "manufacturer_name": ["Dr.Reddy's Laboratories Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE, GLASS (55111-688-52)", "package_ndc": "55111-688-52", "marketing_start_date": "20130403"}], "brand_name": "Zoledronic Acid", "product_id": "55111-688_251add88-5c4f-2750-c713-744fcf3a60ba", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "55111-688", "generic_name": "Zoledronic Acid", "labeler_name": "Dr.Reddy's Laboratories Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA091363", "marketing_category": "ANDA", "marketing_start_date": "20130403", "listing_expiration_date": "20261231"}