zoledronic acid

Generic: zoledronic acid

Labeler: fosun pharma usa inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zoledronic acid
Generic Name zoledronic acid
Labeler fosun pharma usa inc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

zoledronic acid 5 mg/100mL

Manufacturer
FOSUN PHARMA USA INC

Identifiers & Regulatory

Product NDC 72266-152
Product ID 72266-152_181b55f6-9f8c-671b-e063-6394a90a22b3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209578
Listing Expiration 2026-12-31
Marketing Start 2023-06-12

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72266152
Hyphenated Format 72266-152

Supplemental Identifiers

RxCUI
705824
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 ANDA209578 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/100mL
source: ndc
Packaging
  • 1 BAG in 1 CARTON (72266-152-01) / 100 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

zoledronic acid (5 mg/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "181b55f6-9f8c-671b-e063-6394a90a22b3", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["fd0324d8-b9bd-fd4c-e053-6394a90a5465"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 CARTON (72266-152-01)  / 100 mL in 1 BAG", "package_ndc": "72266-152-01", "marketing_start_date": "20230612"}], "brand_name": "Zoledronic acid", "product_id": "72266-152_181b55f6-9f8c-671b-e063-6394a90a22b3", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "72266-152", "generic_name": "Zoledronic acid", "labeler_name": "FOSUN PHARMA USA INC", "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": "20230612", "listing_expiration_date": "20261231"}