Albumin (Human)
These highlights do not include all the information needed to use ALBUMIN (HUMAN) 20% safely and effectively. See full prescribing information for ALBUMIN (HUMAN) 20%. ALBUMIN (HUMAN) 20% For intravenous use only 20% solution Initial U.S. Approval: 2006
Approved
Approval ID
90f0c351-3977-2b84-0a6a-e9cb091430ca
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 1, 2008
Manufacturers
FDA
Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
DUNS: 301119178
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Albumin Human
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67467-633
Application NumberBLA125154
Product Classification
M
Marketing Category
C73585
G
Generic Name
Albumin Human
Product Specifications
Route of AdministrationIntravenous
Effective DateAugust 1, 2008
FDA Product Classification
INGREDIENTS (1)
ALBUMIN (HUMAN)Active
Quantity: 200 g in 1000 mL
Code: ZIF514RVZR
Classification: ACTIB