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ELIQUIS

NDC 0003-1028, apixaban, tablet, for suspension, from E.R. Squibb & Sons, L.L.C..

Product NDC
0003-1028
Status
Listed
Labeler
E.R. Squibb & Sons, L.L.C.
Dosage form
TABLET, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA202155
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0003-1028 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • APIXABAN.5 mg/1

Pharmacologic classes

Factor Xa Inhibitor [EPC]; Factor Xa Inhibitors [MoA]

Package NDCNDC-11Package
0003-1028-120000310281228 PACKET in 1 CARTON (0003-1028-12) / 4 TABLET, FOR SUSPENSION in 1 PACKET
0003-1028-280000310282828 PACKET in 1 CARTON (0003-1028-28) / 1 TABLET, FOR SUSPENSION in 1 PACKET
0003-1028-840000310288428 PACKET in 1 CARTON (0003-1028-84) / 3 TABLET, FOR SUSPENSION in 1 PACKET

Linked data

RxNorm, label and prices

Use it

Look up 0003-1028 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0003-1028 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0003-1028. 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.