zoledronic acid
Generic: zoledronic acid
Labeler: westminster pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
westminster pharmaceuticals, llc
Dosage Form
INJECTION
Routes
Active Ingredients
zoledronic acid 4 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
69367-190
Product ID
69367-190_d8c7e44e-b472-4c33-bfd7-1eb9d18b4a0f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202923
Listing Expiration
2026-12-31
Marketing Start
2023-02-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69367190
Hyphenated Format
69367-190
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
ANDA202923 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/5mL
Packaging
- 1 VIAL in 1 CARTON (69367-190-50) / 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": "d8c7e44e-b472-4c33-bfd7-1eb9d18b4a0f", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["6a153c94-3cb5-4c05-98b2-1e18f5f3fe80"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (69367-190-50) / 5 mL in 1 VIAL", "package_ndc": "69367-190-50", "marketing_start_date": "20230202"}], "brand_name": "Zoledronic Acid", "product_id": "69367-190_d8c7e44e-b472-4c33-bfd7-1eb9d18b4a0f", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "69367-190", "generic_name": "Zoledronic Acid", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA202923", "marketing_category": "ANDA", "marketing_start_date": "20230202", "listing_expiration_date": "20261231"}