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Prednisolone Sodium Phosphate

NDC 68788-7708, Prednisolone Sodium Phosphate, solution, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-7708
Status
Listed
Labeler
Preferred Pharmaceuticals, 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/68788-7708 \
  -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
68788-7708-268788770802237 mL in 1 BOTTLE (68788-7708-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/93b372f7-b811-4c15-85c4-c6dbac342cb4

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=68788-7708

Use it

Look up 68788-7708 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7708 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7708. 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.