zoledronic acid
Generic: zoledronic acid
Labeler: dr. reddy's laboratories incDrug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
dr. reddy's laboratories inc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
zoledronic acid 4 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
43598-255
Product ID
43598-255_9f84a6ad-be66-32f8-d1cc-cc0165058c27
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204344
Listing Expiration
2026-12-31
Marketing Start
2019-01-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598255
Hyphenated Format
43598-255
Supplemental Identifiers
RxCUI
UPC
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
ANDA204344 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/100mL
Packaging
- 1 BOTTLE in 1 CARTON (43598-255-52) / 100 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9f84a6ad-be66-32f8-d1cc-cc0165058c27", "openfda": {"upc": ["0343598255521"], "unii": ["6XC1PAD3KF"], "rxcui": ["1114085"], "spl_set_id": ["b165df31-52f0-d67f-71e7-f3b4f18d2f15"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-255-52) / 100 mL in 1 BOTTLE", "package_ndc": "43598-255-52", "marketing_start_date": "20190115"}], "brand_name": "Zoledronic acid", "product_id": "43598-255_9f84a6ad-be66-32f8-d1cc-cc0165058c27", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "43598-255", "generic_name": "Zoledronic acid", "labeler_name": "Dr. Reddy's Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/100mL"}], "application_number": "ANDA204344", "marketing_category": "ANDA", "marketing_start_date": "20190115", "listing_expiration_date": "20261231"}