Baclofen
These highlights do not include all the information needed to use baclofen oral solution safely and effectively. See full prescribing information for baclofen oral solution. BACLOFEN oral solution Initial U.S. Approval: 1977
Approved
Approval ID
f8ec79c6-da65-4fb6-b6bd-45df0d2a52c7
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 18, 2023
Manufacturers
FDA
TRUPHARMA, LLC
DUNS: 078533947
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Baclofen
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52817-620
Application NumberNDA208193
Product Classification
M
Marketing Category
C73605
G
Generic Name
Baclofen
Product Specifications
Route of AdministrationORAL
Effective DateOctober 18, 2023
FDA Product Classification
INGREDIENTS (6)
PROPYLPARABENInactive
Code: Z8IX2SC1OH
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
METHYLPARABENInactive
Code: A2I8C7HI9T
Classification: IACT
SUCRALOSEInactive
Code: 96K6UQ3ZD4
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
BACLOFENActive
Quantity: 10 mg in 5 mL
Code: H789N3FKE8
Classification: ACTIB