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Prednisolone Sodium Phosphate

NDC 69238-2122, Prednisolone Sodium Phosphate, solution, from Amneal Pharmaceuticals NY LLC.

Product NDC
69238-2122
Status
Listed
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216715
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2122 \
  -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
69238-2122-969238212209237 mL in 1 BOTTLE (69238-2122-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/286a6032-41de-435a-b6e6-14052b66b85d

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=69238-2122

  • NADAC price for package 69238212209

    GET /v1/drugs/nadac/69238212209

Use it

Look up 69238-2122 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2122 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69238-2122. 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.