Product Details for: Plasmanate

RETURN TO SEARCH RESULTS
PRODUCT LABEL Grayed out Product Label links indicate that there is no product label available for the product.
Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
25G/500ML
Single-Dose Vial
351(a)
Plasmanate
Disc
002
Injection
Intravenous
2.5G/50ML
Single-Dose Vial
351(a)
Plasmanate
Disc
003
Injection
Intravenous
12.5G/250ML
Single-Dose Vial
351(a)
Plasmanate
Rx
Proper Name
Plasma Protein Fraction (Human)
BLA Number
101140
Applicant
Grifols Therapeutics LLC
Original Approval Date
October 2, 1958
Date of First Licensure
RETURN TO SEARCH RESULTS