carboplatin

Generic: carboplatin

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name carboplatin
Generic Name carboplatin
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

carboplatin 10 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 61703-339
Product ID 61703-339_0ddf4411-7138-412a-908a-fadf22bdfb79
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076517
Listing Expiration 2026-12-31
Marketing Start 2004-10-14

Pharmacologic Class

Established (EPC)
platinum-based drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61703339
Hyphenated Format 61703-339

Supplemental Identifiers

RxCUI
597195
UNII
BG3F62OND5
NUI
N0000175413 N0000175073

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-18) / 5 mL in 1 VIAL, MULTI-DOSE
  • 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-22) / 15 mL in 1 VIAL, MULTI-DOSE
  • 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-50) / 45 mL in 1 VIAL, MULTI-DOSE
  • 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-56) / 60 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (4)

Ingredients (1)

carboplatin (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0ddf4411-7138-412a-908a-fadf22bdfb79", "openfda": {"nui": ["N0000175413", "N0000175073"], "unii": ["BG3F62OND5"], "rxcui": ["597195"], "spl_set_id": ["c3ae9880-44bb-4f4e-93d8-8a5e21708a30"], "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 (61703-339-18)  / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-339-18", "marketing_start_date": "20041014"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-22)  / 15 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-339-22", "marketing_start_date": "20041014"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-50)  / 45 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-339-50", "marketing_start_date": "20041014"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-56)  / 60 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "61703-339-56", "marketing_start_date": "20041123"}], "brand_name": "Carboplatin", "product_id": "61703-339_0ddf4411-7138-412a-908a-fadf22bdfb79", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "61703-339", "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": "20041014", "listing_expiration_date": "20261231"}