carboplatin
Generic: carboplatin
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
carboplatin
Generic Name
carboplatin
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
carboplatin 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
61703-150
Product ID
61703-150_5aa72c15-8033-4559-b257-373371b18958
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076517
Listing Expiration
2026-12-31
Marketing Start
2022-05-23
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61703150
Hyphenated Format
61703-150
Supplemental Identifiers
RxCUI
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
ANDA076517 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (61703-150-05) / 15 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": "5aa72c15-8033-4559-b257-373371b18958", "openfda": {"nui": ["N0000175413", "N0000175073"], "unii": ["BG3F62OND5"], "rxcui": ["597195"], "spl_set_id": ["47677091-fd20-49af-933c-c9dd2be21de9"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (61703-150-05) / 15 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-150-05", "marketing_start_date": "20220523"}], "brand_name": "Carboplatin", "product_id": "61703-150_5aa72c15-8033-4559-b257-373371b18958", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "61703-150", "generic_name": "Carboplatin", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carboplatin", "active_ingredients": [{"name": "CARBOPLATIN", "strength": "10 mg/mL"}], "application_number": "ANDA076517", "marketing_category": "ANDA", "marketing_start_date": "20220523", "listing_expiration_date": "20261231"}