Drugplain

GoLYTELY 236 g/4L

Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride · POWDER, FOR SOLUTION · Braintree Laboratories, Inc.

No Recall History
Plain English

GoLYTELY is a powder, for solution containing polyethylene glycol 3350, sodium sulfate anhydrous, sodium bicarbonate, sodium chloride, potassium chloride at 236 g/4L, taken oral. Manufactured by Braintree Laboratories, Inc..

Key Facts

Brand Name
GoLYTELY
Generic Name
Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride
NDC Code (Product)
52268-100
Manufacturer
Braintree Laboratories, Inc.
Strength
236 g/4L
Dosage Form
POWDER, FOR SOLUTION
Route
ORAL
Marketing Status
Application #
NDA019011
Drug Class
Osmotic Laxative [EPC]
Marketing Start
07/13/1984

Recall History

No Recall History

Frequently Asked Questions

What is GoLYTELY used for?

GoLYTELY contains Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride. It is a powder, for solution taken oral. Consult your doctor for specific uses.

Is GoLYTELY a controlled substance?

GoLYTELY is not classified as a controlled substance by the DEA.

What is the generic name for GoLYTELY?

The generic name for GoLYTELY is Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride. There are 3 other brand versions of Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride.

What is the NDC code for GoLYTELY 236 g/4L?

The NDC (National Drug Code) for GoLYTELY 236 g/4L is 52268-100, listed by Braintree Laboratories, Inc..

Product NDC

52268-100

Package NDC

52268-100-01

Other GoLYTELY Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)