MOVIPREP
Approved
Approval ID
6ca2803e-a4d6-4e57-a910-13237c93a4ce
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 30, 2009
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, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE and ASCORBIC ACID
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-5890
Application NumberNDA021881
Product Classification
M
Marketing Category
C73594
G
Generic Name
POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE and ASCORBIC ACID
Product Specifications
Effective DateNovember 30, 2009
FDA Product Classification