Rx-Specimen Collection Kit
Rx-Specimen Collection Kit
Approved
Approval ID
a44b385e-7060-4c19-933a-7565319de438
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 22, 2018
Manufacturers
FDA
MAS Management Group Inc.
DUNS: 079363782
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
specimen collection kit
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69677-030
Application NumberANDA078010
Product Classification
M
Marketing Category
C73584
G
Generic Name
specimen collection kit
Product Specifications
Effective DateFebruary 22, 2018
FDA Product Classification