dexrazoxane

Generic: dexrazoxane

Labeler: eugia us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexrazoxane
Generic Name dexrazoxane
Labeler eugia us llc
Dosage Form KIT
Manufacturer
Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-437
Product ID 55150-437_f0a2a9ff-2f1f-481b-96c8-404e9d4a60fa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200752
Listing Expiration 2026-12-31
Marketing Start 2016-05-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150437
Hyphenated Format 55150-437

Supplemental Identifiers

RxCUI
1736585 1736590

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 dexrazoxane (source: ndc)
Generic Name dexrazoxane (source: ndc)
Application Number ANDA200752 (source: ndc)

Resolved Composition

Strengths
  • 250 mg
  • 500 mg
  • 25 ml
  • 50 ml
source: label
Packaging
  • 1 KIT in 1 PACKAGE (55150-437-01) * 50 mL in 1 VIAL, SINGLE-DOSE (55150-435-01) * 50 mL in 1 VIAL (55150-436-01)
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "f0a2a9ff-2f1f-481b-96c8-404e9d4a60fa", "openfda": {"rxcui": ["1736585", "1736590"], "spl_set_id": ["be9ac1e9-21a9-439a-9029-9f03513220ea"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (55150-437-01)  *  50 mL in 1 VIAL, SINGLE-DOSE (55150-435-01)  *  50 mL in 1 VIAL (55150-436-01)", "package_ndc": "55150-437-01", "marketing_start_date": "20160512"}], "brand_name": "DEXRAZOXANE", "product_id": "55150-437_f0a2a9ff-2f1f-481b-96c8-404e9d4a60fa", "dosage_form": "KIT", "product_ndc": "55150-437", "generic_name": "DEXRAZOXANE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXRAZOXANE", "application_number": "ANDA200752", "marketing_category": "ANDA", "marketing_start_date": "20160512", "listing_expiration_date": "20261231"}