zoledronic acid

Generic: zoledronic acid

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zoledronic acid
Generic Name zoledronic acid
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

zoledronic acid 4 mg/5mL

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-170
Product ID 23155-170_f4991976-8a87-4a00-839f-3f62c561c230
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201783
Listing Expiration 2026-12-31
Marketing Start 2023-08-31

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155170
Hyphenated Format 23155-170

Supplemental Identifiers

RxCUI
351114
UPC
0323155170313
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 ANDA201783 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4 mg/5mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (23155-170-31) / 5 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (1)

zoledronic acid (4 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f4991976-8a87-4a00-839f-3f62c561c230", "openfda": {"upc": ["0323155170313"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["00a5bd5a-e5ee-4bad-b510-a4d4485485c8"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (23155-170-31)  / 5 mL in 1 VIAL, GLASS", "package_ndc": "23155-170-31", "marketing_start_date": "20230831"}], "brand_name": "Zoledronic acid", "product_id": "23155-170_f4991976-8a87-4a00-839f-3f62c561c230", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "23155-170", "generic_name": "Zoledronic acid", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA201783", "marketing_category": "ANDA", "marketing_start_date": "20230831", "listing_expiration_date": "20261231"}