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PREDNISONE

NDC 68071-3738, PREDNISONE, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3738
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215672
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3738 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-3738-16807137380110 TABLET in 1 BOTTLE (68071-3738-1)
68071-3738-3680713738033 TABLET in 1 BOTTLE (68071-3738-3)
68071-3738-4680713738044 TABLET in 1 BOTTLE (68071-3738-4)
68071-3738-6680713738066 TABLET in 1 BOTTLE (68071-3738-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/288ecb6d-3b0b-db95-e063-6394a90a78ff

Use it

Look up 68071-3738 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3738 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3738. 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.