52268-101 : Golytely Oral Powder, for Solution


NDC52268-101
Labeler: Braintree Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Golytely
Dosage Form: Oral Powder, for Solution
Application #: NDA019011
Rev. Date: 


NDC Package Codes:

  • 52268-101-01: 4 L IN 1 BOTTLE, PLASTIC (52268‑101‑01)

Active Ingredients:

  • Polyethylene Glycol 3350
  • Potassium Chloride
  • Sodium Bicarbonate
  • Sodium Chloride
  • Sodium Sulfate Anhydrous

Dosage Strength:

  • 236 g/4L
  • 2.97 g/4L
  • 6.74 g/4L
  • 5.86 g/4L
  • 22.74 g/4L

Pharmaceutical Classes:

  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Potassium Compounds [CS]
  • Potassium Salt [EPC]

Related Products:

Based on records with the same trade name.
  • 52268-100 Golytely Oral Powder, for Solution by Braintree Laboratories, Inc.
  • 52268-700 Golytely Oral Powder, for Solution by Braintree Laboratories, Inc.
  • 54868-0054 Golytely Nasogastric; Oral Powder, for Solution by Physicians Total Care, Inc.

NDC QR Code

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