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TRILYTE

NDC 84386-013, polyethylene glyocol 3350, sodium chloride, sodium bicarbonate and potassium chloride, powder, for solution, from Aurobindo Pharma Limited.

Product NDC
84386-013
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076491
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/84386-013 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POLYETHYLENE GLYCOL 3350420 g/4L
  • SODIUM BICARBONATE5.72 g/4L
  • SODIUM CHLORIDE11.2 g/4L
  • POTASSIUM CHLORIDE1.48 g/4L

Pharmacologic classes

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

Package NDCNDC-11Package
84386-013-04843860013044 L in 1 BOTTLE (84386-013-04)

Linked data

RxNorm, label and prices

Use it

Look up 84386-013 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/84386-013 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 84386-013. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.