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Prednisolone Sodium Phosphate

NDC 70518-4524, Prednisolone Sodium Phosphate, solution, from REMEDYREPACK INC..

Product NDC
70518-4524
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076913
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4524 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE15 mg/5mL

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
70518-4524-0705184524002 CUP in 1 BOX (70518-4524-0) / 25 mL in 1 CUP (70518-4524-1)
70518-4524-2705184524025 CUP in 1 BOX (70518-4524-2) / 10 mL in 1 CUP (70518-4524-3)
70518-4524-47051845240410 CUP in 1 BOX (70518-4524-4) / 5 mL in 1 CUP (70518-4524-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f87ce1ba-335e-463d-87d5-9af0206f8f61

Use it

Look up 70518-4524 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4524 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4524. 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.