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 .25 g/mL

Manufacturer
BPL

Identifiers & Regulatory

Product NDC 64208-2512
Product ID 64208-2512_85f1cecd-a23d-498f-adfb-0a09feed1994
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 642082512
Hyphenated Format 64208-2512

Supplemental Identifiers

RxCUI
2054168 2054170 2054173 2054174
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
  • .25 g/mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (64208-2512-3) / 50 mL in 1 VIAL, GLASS (64208-2512-4)
  • 1 VIAL, GLASS in 1 CARTON (64208-2512-7) / 100 mL in 1 VIAL, GLASS (64208-2512-8)
source: ndc

Packages (2)

Ingredients (1)

albumin human (.25 g/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "85f1cecd-a23d-498f-adfb-0a09feed1994", "openfda": {"unii": ["ZIF514RVZR"], "rxcui": ["2054168", "2054170", "2054173", "2054174"], "spl_set_id": ["167f48d0-8ae5-4f7e-b050-9673dad78acc"], "manufacturer_name": ["BPL"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (64208-2512-3)  / 50 mL in 1 VIAL, GLASS (64208-2512-4)", "package_ndc": "64208-2512-3", "marketing_start_date": "20200527"}, {"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (64208-2512-7)  / 100 mL in 1 VIAL, GLASS (64208-2512-8)", "package_ndc": "64208-2512-7", "marketing_start_date": "20200527"}], "brand_name": "ALBUMINEX", "product_id": "64208-2512_85f1cecd-a23d-498f-adfb-0a09feed1994", "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": "64208-2512", "generic_name": "Albumin Human", "labeler_name": "BPL", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUMINEX", "active_ingredients": [{"name": "ALBUMIN HUMAN", "strength": ".25 g/mL"}], "application_number": "BLA125644", "marketing_category": "BLA", "marketing_start_date": "20200527", "listing_expiration_date": "20261231"}