palonosetron
Generic: palonosetron
Labeler: bluepoint laboratoriesDrug Facts
Product Profile
Brand Name
palonosetron
Generic Name
palonosetron
Labeler
bluepoint laboratories
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
palonosetron hydrochloride .05 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68001-355
Product ID
68001-355_2cefd5b7-b32d-7b91-e063-6394a90af3b8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201533
Listing Expiration
2026-12-31
Marketing Start
2018-05-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68001355
Hyphenated Format
68001-355
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
palonosetron (source: ndc)
Generic Name
palonosetron (source: ndc)
Application Number
ANDA201533 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .05 mg/mL
Packaging
- 1 VIAL, SINGLE-USE in 1 CARTON (68001-355-25) / 5 mL in 1 VIAL, SINGLE-USE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2cefd5b7-b32d-7b91-e063-6394a90af3b8", "openfda": {"upc": ["0368001355254"], "unii": ["23310D4I19"], "rxcui": ["1728055"], "spl_set_id": ["ee6f6f94-1ca7-481e-9909-b19ae64e80c2"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (68001-355-25) / 5 mL in 1 VIAL, SINGLE-USE", "package_ndc": "68001-355-25", "marketing_start_date": "20180530"}], "brand_name": "Palonosetron", "product_id": "68001-355_2cefd5b7-b32d-7b91-e063-6394a90af3b8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68001-355", "generic_name": "Palonosetron", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Palonosetron", "active_ingredients": [{"name": "PALONOSETRON HYDROCHLORIDE", "strength": ".05 mg/mL"}], "application_number": "ANDA201533", "marketing_category": "ANDA", "marketing_start_date": "20180530", "listing_expiration_date": "20261231"}