albuminex
Generic: albumin human
Labeler: bplDrug Facts
Product Profile
Brand Name
albuminex
Generic Name
albumin human
Labeler
bpl
Dosage Form
SOLUTION
Routes
Active Ingredients
albumin human .25 g/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
642082512
Hyphenated Format
64208-2512
Supplemental Identifiers
RxCUI
UNII
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
albuminex (source: ndc)
Generic Name
albumin human (source: ndc)
Application Number
BLA125644 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .25 g/mL
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)
Packages (2)
Ingredients (1)
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"}