52268-700 : Golytely Oral Powder, for Solution


NDC: 52268-700
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:

  • 52268-700-01: 4 L IN 1 PACKET (52268‑700‑01)

Active Ingredients:

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

Dosage Strength:

  • 227.1 g/L
  • 21.5 g/L
  • 6.36 g/L
  • 5.53 g/L
  • .754 g/L

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.
  • 52268-101 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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NDC 52268-700 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.