carboplatin
Generic: carboplatin
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
carboplatin
Generic Name
carboplatin
Labeler
eugia us llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
carboplatin 50 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
55150-333
Product ID
55150-333_6029d051-ee8d-44cc-8dae-b91c3385d4c3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205487
Listing Expiration
2026-12-31
Marketing Start
2016-09-29
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150333
Hyphenated Format
55150-333
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
carboplatin (source: ndc)
Generic Name
carboplatin (source: ndc)
Application Number
ANDA205487 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/5mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (55150-333-01) / 5 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6029d051-ee8d-44cc-8dae-b91c3385d4c3", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0355150334018", "0355150333011"], "unii": ["BG3F62OND5"], "rxcui": ["597195"], "spl_set_id": ["f5fe9a20-47a5-45b9-ab06-c6158d9b6aca"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (55150-333-01) / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-333-01", "marketing_start_date": "20160929"}], "brand_name": "CARBOPLATIN", "product_id": "55150-333_6029d051-ee8d-44cc-8dae-b91c3385d4c3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "55150-333", "generic_name": "CARBOPLATIN", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CARBOPLATIN", "active_ingredients": [{"name": "CARBOPLATIN", "strength": "50 mg/5mL"}], "application_number": "ANDA205487", "marketing_category": "ANDA", "marketing_start_date": "20160929", "listing_expiration_date": "20261231"}