zoledronic acid
Generic: zoledronic acid
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
zoledronic acid 5 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-806
Product ID
71288-806_a4589df5-8c10-4040-ba54-637c518a0e11
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213371
Listing Expiration
2026-12-31
Marketing Start
2023-06-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288806
Hyphenated Format
71288-806
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
ANDA213371 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/100mL
Packaging
- 1 BOTTLE, GLASS in 1 CARTON (71288-806-51) / 100 mL in 1 BOTTLE, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a4589df5-8c10-4040-ba54-637c518a0e11", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["8aac81ae-f92c-4f0b-b480-44badf72b5f5"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (71288-806-51) / 100 mL in 1 BOTTLE, GLASS", "package_ndc": "71288-806-51", "marketing_start_date": "20230605"}], "brand_name": "Zoledronic Acid", "product_id": "71288-806_a4589df5-8c10-4040-ba54-637c518a0e11", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "71288-806", "generic_name": "Zoledronic Acid", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA213371", "marketing_category": "ANDA", "marketing_start_date": "20230605", "listing_expiration_date": "20261231"}