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Pantoprazole Sodium

NDC 48433-081, pantoprazole sodium, tablet, delayed release, from Safecor Health LLC.

Product NDC
48433-081
Status
Listed
Labeler
Safecor Health LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090970
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/48433-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM40 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
48433-081-2048433008120100 BLISTER PACK in 1 CARTON (48433-081-20) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (48433-081-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5e1cbf26-d379-4315-8732-3939968f32c0

Use it

Look up 48433-081 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/48433-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 48433-081. 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.