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PANTOPRAZOLE SODIUM

NDC 62332-071, pantoprazole sodium injection, powder, for solution, from Alembic Pharmaceuticals Inc..

Product NDC
62332-071
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
POWDER, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219230
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-071 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM40 mg/10mL

Pharmacologic classes

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

Package NDCNDC-11Package
62332-071-01623320071011 VIAL in 1 CARTON (62332-071-01) / 10 mL in 1 VIAL
62332-071-106233200711010 VIAL in 1 CARTON (62332-071-10) / 10 mL in 1 VIAL
62332-071-256233200712525 VIAL in 1 CARTON (62332-071-25) / 10 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a9e5fac6-2db6-4311-a98b-eb3f0dde19d6

Use it

Look up 62332-071 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-071 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-071. 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.