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PANTOPRAZOLE SODIUM

NDC 62756-071, PANTOPRAZOLE SODIUM, granule, delayed release, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-071
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
GRANULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213725
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-071 \
  -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
62756-071-646275600716430 PACKET in 1 CARTON (62756-071-64) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (62756-071-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/38353b9e-63bd-47e8-b7cb-b198d1e901f9

  • NADAC price for package 62756007164

    GET /v1/drugs/nadac/62756007164

Use it

Look up 62756-071 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-071 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-071. 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.