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SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE

NDC 52536-177, sodium sulfate, potassium sulfate, magnesium sulfate, solution, concentrate, from Wilshire Pharmaceuticals, Inc..

Product NDC
52536-177
Status
Listed
Labeler
Wilshire Pharmaceuticals, Inc.
Dosage form
SOLUTION, CONCENTRATE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA022372
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52536-177 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM SULFATE13.13 g/133.1mL
  • POTASSIUM SULFATE2.35 g/133.1mL
  • MAGNESIUM SULFATE, UNSPECIFIED FORM1.2 g/133.1mL

Pharmacologic classes

Calculi Dissolution Agent [EPC]; 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]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; 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
52536-177-01525360177012 BOTTLE, PLASTIC in 1 CARTON (52536-177-01) / 133.1 mL in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f269929e-c2ff-4288-9d3b-7770bcb5a498

Use it

Look up 52536-177 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52536-177 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52536-177. 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.