52268-302 : Nulytely Oral Powder, for Solution


NDC: 52268-302
Labeler: Braintree Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Nulytely
Dosage Form: Oral Powder, for Solution
Application #: NDA019797
Rev. Date: 


NDC Package Codes:

  • 52268-302-01: 4 L IN 1 PACKAGE (52268‑302‑01)

Active Ingredients:

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

Dosage Strength:

  • 420 g/4L
  • 5.72 g/4L
  • 11.2 g/4L
  • 1.48 g/4L

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 52268-400 Nulytely Oral Powder, for Solution by Braintree Laboratories, Inc.
  • 54868-4233 Nulytely Oral Powder, for Solution by Physicians Total Care, Inc.

NDC 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.