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Prednisolone Sodium Phosphate

NDC 68999-330, prednisolone sodium phosphate, solution, from Chartwell Governmental & Specialty RX, LLC..

Product NDC
68999-330
Status
Listed
Labeler
Chartwell Governmental & Specialty RX, LLC.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075988
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68999-330 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE5 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
68999-330-24689990330242 TRAY in 1 BOX (68999-330-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-330-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5ec401b5-132a-4cd2-8c24-6a5c8b63c2f9

Use it

Look up 68999-330 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68999-330 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68999-330. 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.