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PREDNISOLONE SODIUM PHOSPHATE

NDC 24208-715, PREDNISOLONE SODIUM PHOSPHATE, solution/ drops, from Bausch & Lomb Incorporated.

Product NDC
24208-715
Status
Listed
Labeler
Bausch & Lomb Incorporated
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040070
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24208-715 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE10 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
24208-715-10242080715101 BOTTLE, DROPPER in 1 CARTON (24208-715-10) / 10 mL in 1 BOTTLE, DROPPER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8a7f0f2a-3a48-4488-89cd-3e91c3b1365f

  • NADAC price for package 24208071510

    GET /v1/drugs/nadac/24208071510

Use it

Look up 24208-715 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24208-715 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24208-715. 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.