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Prednisolone Sodium Phosphate Oral Solution

NDC 44523-182, Prednisolone Sodium Phosphate, solution, from BioComp Pharma, Inc..

Product NDC
44523-182
Status
Listed
Labeler
BioComp Pharma, Inc.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091396
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/44523-182 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE25 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
44523-182-0844523018208237 mL in 1 BOTTLE (44523-182-08)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/95208441-1700-5d3f-e053-2a95a90a7da2

Use it

Look up 44523-182 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/44523-182 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 44523-182. 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.