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Prednisone delayed release

NDC 43598-887, Prednisone, tablet, delayed release, from Dr. Reddys Laboratories Inc..

Product NDC
43598-887
Status
Listed
Labeler
Dr. Reddys Laboratories Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219477
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-887 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
43598-887-30435980887301 BOTTLE in 1 CARTON (43598-887-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/01bdc479-1f1f-af94-837c-12e7e861321a

Use it

Look up 43598-887 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-887 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-887. 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.