zoledronic acid
Generic: zoledronic acid
Labeler: bluepoint laboratoriesDrug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
bluepoint laboratories
Dosage Form
INJECTION
Routes
Active Ingredients
zoledronic acid 5 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
68001-611
Product ID
68001-611_1f29ce94-b284-836a-e063-6294a90aa50b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209578
Listing Expiration
2026-12-31
Marketing Start
2024-03-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68001611
Hyphenated Format
68001-611
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
ANDA209578 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/100mL
Packaging
- 1 BAG in 1 CARTON (68001-611-33) / 100 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1f29ce94-b284-836a-e063-6294a90aa50b", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["5de65a7f-a219-4b22-9155-61fedc84433b"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 CARTON (68001-611-33) / 100 mL in 1 BAG", "package_ndc": "68001-611-33", "marketing_start_date": "20240706"}], "brand_name": "Zoledronic acid", "product_id": "68001-611_1f29ce94-b284-836a-e063-6294a90aa50b", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68001-611", "generic_name": "Zoledronic acid", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA209578", "marketing_category": "ANDA", "marketing_start_date": "20240308", "listing_expiration_date": "20261231"}