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Pantoprazole Sodium

NDC 85509-1636, Pantoprazole, tablet, delayed release, from PHOENIX RX LLC.

Product NDC
85509-1636
Status
Listed
Labeler
PHOENIX RX LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205119
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1636 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
85509-1636-38550916360330 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1636-3)
85509-1636-68550916360660 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1636-6)
85509-1636-98550916360990 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1636-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/440b9ae8-2fb8-5d35-e063-6294a90a82b6

Use it

Look up 85509-1636 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1636 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85509-1636. 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.