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Rabeprazole Sodium

NDC 71205-292, Rabeprazole Sodium, tablet, delayed release, from Proficient Rx LP.

Product NDC
71205-292
Status
Listed
Labeler
Proficient Rx LP
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/71205-292 \
  -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
71205-292-03712050292033 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-03)
71205-292-307120502923030 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-30)
71205-292-607120502926060 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-60)
71205-292-907120502929090 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/68b7a793-f22b-4609-a640-94fdec703d93

Use it

Look up 71205-292 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-292 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-292. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.