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prednisolone sodium phosphate ODT

NDC 50742-385, prednisolone sodium phosphate, tablet, orally disintegrating, from Ingenus Pharmaceuticals, LLC.

Product NDC
50742-385
Status
Listed
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021959
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50742-385 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50742-385-12507420385122 BLISTER PACK in 1 CARTON (50742-385-12) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50742-385-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ebbc1751-9381-4db1-89ff-ae5a2963fb2c

Use it

Look up 50742-385 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50742-385 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50742-385. 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.