melphalan hydrochloride
Melphalan Hydrochloride for Injection Rx only
Approved
Approval ID
a981ddb1-d05a-2cfe-10f5-1ce4dad8fe3c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 8, 2023
Manufacturers
FDA
Almaject, Inc.
DUNS: 116626205
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
melphalan hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72611-779
Application NumberANDA204817
Product Classification
M
Marketing Category
C73584
G
Generic Name
melphalan hydrochloride
Product Specifications
Effective DateMay 20, 2015
FDA Product Classification