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prednisone

NDC 71205-818, prednisone, tablet, from Proficient Rx LP.

Product NDC
71205-818
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213386
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-818 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-818-05712050818055 TABLET in 1 BOTTLE, PLASTIC (71205-818-05)
71205-818-06712050818066 TABLET in 1 BOTTLE, PLASTIC (71205-818-06)
71205-818-07712050818077 TABLET in 1 BOTTLE, PLASTIC (71205-818-07)
71205-818-107120508181010 TABLET in 1 BOTTLE, PLASTIC (71205-818-10)
71205-818-127120508181212 TABLET in 1 BOTTLE, PLASTIC (71205-818-12)
71205-818-147120508181414 TABLET in 1 BOTTLE, PLASTIC (71205-818-14)
71205-818-157120508181515 TABLET in 1 BOTTLE, PLASTIC (71205-818-15)
71205-818-207120508182020 TABLET in 1 BOTTLE, PLASTIC (71205-818-20)
71205-818-217120508182121 TABLET in 1 BOTTLE, PLASTIC (71205-818-21)
71205-818-247120508182424 TABLET in 1 BOTTLE, PLASTIC (71205-818-24)
71205-818-287120508182828 TABLET in 1 BOTTLE, PLASTIC (71205-818-28)
71205-818-307120508183030 TABLET in 1 BOTTLE, PLASTIC (71205-818-30)
71205-818-407120508184040 TABLET in 1 BOTTLE, PLASTIC (71205-818-40)
71205-818-427120508184242 TABLET in 1 BOTTLE, PLASTIC (71205-818-42)
71205-818-607120508186060 TABLET in 1 BOTTLE, PLASTIC (71205-818-60)
71205-818-907120508189090 TABLET in 1 BOTTLE, PLASTIC (71205-818-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6ec5b58c-65e9-47ee-b2ac-7d0b395a0630

Use it

Look up 71205-818 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-818 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-818. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.