Polyethylene Glycol 3350
Polyethylene Glycol 3350 NF Polyethylene Glycol 3350 Powder for Oral Solution
Approved
Approval ID
d0d2f068-4453-4ea2-8282-339b6e497a9a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 10, 2011
Manufacturers
FDA
Nexgen Pharma, Inc.
DUNS: 048488621
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
NDC Product Code0722-6921
Application NumberANDA077706
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateAugust 10, 2011
Generic NamePolyethylene Glycol 3350
INGREDIENTS (1)
POLYETHYLENE GLYCOL 3350Active
Quantity: 17 g in 1 1
Code: G2M7P15E5P
Classification: ACTIB