zoledronic acid

Generic: zoledronic acid

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zoledronic acid
Generic Name zoledronic acid
Labeler bluepoint laboratories
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

zoledronic acid 4 mg/5mL

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-437
Product ID 68001-437_0179cc91-4a11-1cc0-e063-6294a90a6c1e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205279
Listing Expiration 2026-12-31
Marketing Start 2020-06-29

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001437
Hyphenated Format 68001-437

Supplemental Identifiers

RxCUI
351114
UPC
0368001437257
UNII
6XC1PAD3KF

Packaging Origin

Original Packager
true

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 ANDA205279 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4 mg/5mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (68001-437-25) / 5 mL in 1 VIAL
source: ndc

Packages (1)

68001-437-25 1 VIAL in 1 CARTON (68001-437-25) / 5 mL in 1 VIAL

Ingredients (1)

zoledronic acid (4 mg/5mL)

Linked Drug Pages (1)

Zoledronic acid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0179cc91-4a11-1cc0-e063-6294a90a6c1e", "openfda": {"upc": ["0368001437257"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["666b1833-ee9b-4a6f-bd4c-9526552cec0a"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-437-25)  / 5 mL in 1 VIAL", "package_ndc": "68001-437-25", "marketing_start_date": "20200629"}], "brand_name": "Zoledronic acid", "product_id": "68001-437_0179cc91-4a11-1cc0-e063-6294a90a6c1e", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68001-437", "generic_name": "zoledronic acid", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA205279", "marketing_category": "ANDA", "marketing_start_date": "20200629", "listing_expiration_date": "20261231"}