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Rabeprazole Sodium

NDC 85509-1443, Rabeprazole Sodium, tablet, delayed release, from PHOENIX RX LLC.

Product NDC
85509-1443
Status
Listed
Labeler
PHOENIX RX LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208644
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1443 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RABEPRAZOLE SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
85509-1443-38550914430330 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1443-3)
85509-1443-68550914430660 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1443-6)
85509-1443-98550914430990 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1443-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3a674849-b2f6-5f43-e063-6294a90a9e20

Use it

Look up 85509-1443 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1443 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85509-1443. 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.