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MAGNESIUM SULFATE

NDC 47335-992, magnesium sulfate heptahydrate, injection, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-992
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213917
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-992 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MAGNESIUM SULFATE HEPTAHYDRATE40 mg/mL

Pharmacologic classes

Calculi Dissolution Agent [EPC]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Package NDCNDC-11Package
47335-992-014733509920124 POUCH in 1 CASE (47335-992-01) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
47335-992-024733509920224 POUCH in 1 CASE (47335-992-02) / 1 BAG in 1 POUCH / 100 mL in 1 BAG

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/efadcb55-f935-4c60-b2e2-0a76b9194b50

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=47335-992

Use it

Look up 47335-992 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-992 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-992. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.