zoledronic acid
Generic: zoledronic acid
Labeler: mylan institutional llcDrug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
mylan institutional llc
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
zoledronic acid 4 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
67457-390
Product ID
67457-390_fee40fb6-3020-4f12-9c5d-ad4ce9996028
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202650
Listing Expiration
2027-12-31
Marketing Start
2014-03-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67457390
Hyphenated Format
67457-390
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
zoledronic acid (source: ndc)
Generic Name
zoledronic acid (source: ndc)
Application Number
ANDA202650 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/5mL
Packaging
- 1 VIAL in 1 CARTON (67457-390-54) / 5 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fee40fb6-3020-4f12-9c5d-ad4ce9996028", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["20cd29cc-cef5-48c4-adfe-6b3dfee0ab61"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (67457-390-54) / 5 mL in 1 VIAL", "package_ndc": "67457-390-54", "marketing_start_date": "20140310"}], "brand_name": "Zoledronic acid", "product_id": "67457-390_fee40fb6-3020-4f12-9c5d-ad4ce9996028", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "67457-390", "generic_name": "Zoledronic acid", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA202650", "marketing_category": "ANDA", "marketing_start_date": "20140310", "listing_expiration_date": "20271231"}