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PANTOPRAZOLE SODIUM

NDC 46708-071, pantoprazole sodium injection, powder, for solution, from Alembic Pharmaceuticals Limited.

Product NDC
46708-071
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
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/46708-071 \
  -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
46708-071-01467080071011 VIAL in 1 CARTON (46708-071-01) / 10 mL in 1 VIAL
46708-071-104670800711010 VIAL in 1 CARTON (46708-071-10) / 10 mL in 1 VIAL
46708-071-254670800712525 VIAL in 1 CARTON (46708-071-25) / 10 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/02ee7ed6-217f-4128-bbbb-b9390475a65b

Use it

Look up 46708-071 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-071 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-071. 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.