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Magnesium Sulfate

NDC 70518-4375, MAGNESIUM SULFATE HEPTAHYDRATE, injection, solution, from REMEDYREPACK INC..

Product NDC
70518-4375
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA019316
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4375 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MAGNESIUM SULFATE HEPTAHYDRATE500 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
70518-4375-07051843750025 VIAL, SINGLE-DOSE in 1 TRAY (70518-4375-0) / 10 mL in 1 VIAL, SINGLE-DOSE (70518-4375-1)
70518-4375-27051843750225 VIAL, SINGLE-DOSE in 1 CARTON (70518-4375-2) / 2 mL in 1 VIAL, SINGLE-DOSE (70518-4375-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8c6b8b3d-9c04-4ed7-86b8-89065b6bf50d

Use it

Look up 70518-4375 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4375 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4375. 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.