51525-6831 : Trilyte Nasogastric; Oral Powder, for Solution
| NDC: | 51525-6831 |
| Labeler: | Wallace Pharmaceuticals Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Trilyte With Flavor Packs |
| Dosage Form: | Nasogastric; Oral Powder, for Solution |
| Application #: | ANDA076491 |
| Rev. Date: |
NDC Package Codes:
- 51525-6831-4: 4 L IN 1 BOTTLE (51525‑6831‑4)
Active Ingredients:
- Polyethylene Glycol 3350
- Potassium Chloride
- Sodium Bicarbonate
- Sodium Chloride
Dosage Strength:
- 420 g/4L
- 1.48 g/4L
- 5.72 g/4L
- 11.2 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.- 68220-131 Trilyte Nasogastric; Oral Powder, for Solution by Alaven Pharmaceutical LLC
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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.