albuminex

Generic: albumin human

Labeler: bpl
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name albuminex
Generic Name albumin human
Labeler bpl
Dosage Form SOLUTION
Routes
INTRAVENOUS
Active Ingredients

albumin human .05 g/mL

Manufacturer
BPL

Identifiers & Regulatory

Product NDC 64208-2510
Product ID 64208-2510_7a994321-a724-4f00-a7e7-95dca159394f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA125644
Listing Expiration 2026-12-31
Marketing Start 2020-05-27

Pharmacologic Class

Classes
human serum albumin [epc] increased intravascular volume [pe] increased oncotic pressure [pe] osmotic activity [moa] serum albumin [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 642082510
Hyphenated Format 64208-2510

Supplemental Identifiers

RxCUI
2054221 2054223 2054226 2054227
UNII
ZIF514RVZR

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 albuminex (source: ndc)
Generic Name albumin human (source: ndc)
Application Number BLA125644 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .05 g/mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (64208-2510-1) / 250 mL in 1 VIAL, GLASS (64208-2510-2)
  • 1 VIAL, GLASS in 1 CARTON (64208-2510-5) / 500 mL in 1 VIAL, GLASS (64208-2510-6)
source: ndc

Packages (2)

Ingredients (1)

albumin human (.05 g/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "7a994321-a724-4f00-a7e7-95dca159394f", "openfda": {"unii": ["ZIF514RVZR"], "rxcui": ["2054221", "2054223", "2054226", "2054227"], "spl_set_id": ["8428d373-f4b1-4e3b-bb19-ea89048f7c79"], "manufacturer_name": ["BPL"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (64208-2510-1)  / 250 mL in 1 VIAL, GLASS (64208-2510-2)", "package_ndc": "64208-2510-1", "marketing_start_date": "20200527"}, {"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (64208-2510-5)  / 500 mL in 1 VIAL, GLASS (64208-2510-6)", "package_ndc": "64208-2510-5", "marketing_start_date": "20200527"}], "brand_name": "ALBUMINEX", "product_id": "64208-2510_7a994321-a724-4f00-a7e7-95dca159394f", "dosage_form": "SOLUTION", "pharm_class": ["Human Serum Albumin [EPC]", "Increased Intravascular Volume [PE]", "Increased Oncotic Pressure [PE]", "Osmotic Activity [MoA]", "Serum Albumin [Chemical/Ingredient]"], "product_ndc": "64208-2510", "generic_name": "Albumin Human", "labeler_name": "BPL", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUMINEX", "active_ingredients": [{"name": "ALBUMIN HUMAN", "strength": ".05 g/mL"}], "application_number": "BLA125644", "marketing_category": "BLA", "marketing_start_date": "20200527", "listing_expiration_date": "20261231"}