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RABEPRAZOLE SODIUM

NDC 71205-603, rabeprazole sodium, tablet, delayed release, from Proficient Rx LP.

Product NDC
71205-603
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204237
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-603 \
  -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
71205-603-307120506033030 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-603-30)
71205-603-607120506036060 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-603-60)
71205-603-907120506039090 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-603-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f5eb1b4-ad4b-4782-8d3d-cd33f9c5be7d

Use it

Look up 71205-603 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-603 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-603. 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.