Leukotrap
Approved
Approval ID
028e6f14-34f2-49f4-99a5-83c457d4e96f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 29, 2014
Manufacturers
FDA
Haemonetics Manufacturing Inc
DUNS: 078598396
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Blood Collection System
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code53157-129
Application NumberNDA820915
Product Classification
M
Marketing Category
C73594
G
Generic Name
Blood Collection System
Product Specifications
Effective DateSeptember 29, 2014
FDA Product Classification