POLYETHYLENE GLYCOL 3350
Polyethylene Glycol 3350, NF Powder for Oral Solution
Approved
Approval ID
aa3bc313-3c42-4d4d-bfac-5215def68dab
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 1, 2012
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
POLYETHYLENE GLYCOL 3350
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-5160
Application NumberANDA076652
Product Classification
M
Marketing Category
C73584
G
Generic Name
POLYETHYLENE GLYCOL 3350
Product Specifications
Route of AdministrationORAL
Effective DateMay 1, 2012
FDA Product Classification
INGREDIENTS (1)
POLYETHYLENE GLYCOL 3350Active
Quantity: 1 g in 1 g
Code: G2M7P15E5P
Classification: ACTIB