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VIJOICE

NDC 0078-1021, alpelisib, tablet, from Novartis Pharmaceuticals Corporation.

Product NDC
0078-1021
Status
Listed
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA215039
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0078-1021 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALPELISIB50 mg/1
Package NDCNDC-11Package
0078-1021-84000781021841 BLISTER PACK in 1 CARTON (0078-1021-84) / 28 TABLET in 1 BLISTER PACK (0078-1021-51)
0078-1021-91000781021911 BLISTER PACK in 1 CARTON (0078-1021-91) / 28 TABLET in 1 BLISTER PACK (0078-1021-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/638069a4-aee0-46c9-9e21-54ad449c163c

Use it

Look up 0078-1021 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0078-1021 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0078-1021. 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.