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Prednisolone

NDC 70404-077, Prednisolone oral, solution, from Tulex Pharmaceuticals Inc.

Product NDC
70404-077
Status
Listed
Labeler
Tulex Pharmaceuticals Inc
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219509
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70404-077 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE15 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
70404-077-1470404007714240 mL in 1 BOTTLE (70404-077-14)
70404-077-1670404007716480 mL in 1 BOTTLE (70404-077-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/757b41c4-a0fe-4a09-8816-a4cdb7558f41

Use it

Look up 70404-077 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70404-077 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70404-077. 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.