zoledronic acid
Generic: zoledronic acid
Labeler: dr. reddy's laboratories limitedDrug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
dr. reddy's laboratories limited
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
zoledronic acid 4 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
55111-685
Product ID
55111-685_f524daa0-1742-f647-b08e-46a0477c1540
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091186
Listing Expiration
2026-12-31
Marketing Start
2013-03-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55111685
Hyphenated Format
55111-685
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
ANDA091186 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/5mL
Packaging
- 1 VIAL, GLASS in 1 CARTON (55111-685-07) / 5 mL in 1 VIAL, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f524daa0-1742-f647-b08e-46a0477c1540", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["1738a682-5903-b675-3a7a-61d299a6f248"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (55111-685-07) / 5 mL in 1 VIAL, GLASS", "package_ndc": "55111-685-07", "marketing_start_date": "20130304"}], "brand_name": "Zoledronic Acid", "product_id": "55111-685_f524daa0-1742-f647-b08e-46a0477c1540", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "55111-685", "generic_name": "Zoledronic Acid", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA091186", "marketing_category": "ANDA", "marketing_start_date": "20130304", "listing_expiration_date": "20261231"}