Polyethylene Glycol 3350
Polyethylene Glycol 3350 NF Polyethylene Glycol 3350 Powder for Oral Solution
Approved
Approval ID
a71759de-123d-4984-93e6-35661ad7d739
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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0722-6920
Application NumberANDA077706
Product Classification
M
Marketing Category
C73584
G
Generic Name
Polyethylene Glycol 3350
Product Specifications
Route of AdministrationORAL
Effective DateAugust 10, 2011
FDA Product Classification
INGREDIENTS (1)
POLYETHYLENE GLYCOL 3350Active
Quantity: 17 g in 1 1
Code: G2M7P15E5P
Classification: ACTIB