zoledronic acid
Generic: zoledronic acid
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
zoledronic acid 5 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-966
Product ID
63323-966_9fb5ae91-44b4-4b48-aaeb-0a2ba676aa16
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204217
Listing Expiration
2026-12-31
Marketing Start
2017-02-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323966
Hyphenated Format
63323-966
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
ANDA204217 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/100mL
Packaging
- 1 VIAL, GLASS in 1 CARTON (63323-966-00) / 100 mL in 1 VIAL, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9fb5ae91-44b4-4b48-aaeb-0a2ba676aa16", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["16fcf8c9-ef8a-4e93-9ee6-acfadd35a861"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (63323-966-00) / 100 mL in 1 VIAL, GLASS", "package_ndc": "63323-966-00", "marketing_start_date": "20170217"}], "brand_name": "Zoledronic Acid", "product_id": "63323-966_9fb5ae91-44b4-4b48-aaeb-0a2ba676aa16", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "63323-966", "generic_name": "Zoledronic Acid", "labeler_name": "Fresenius Kabi USA, LLC", "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": "20170217", "listing_expiration_date": "20261231"}