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Pantoprazole sodium delayed-release

NDC 70756-018, Pantoprazole sodium delayed-release, tablet, from Lifestar Pharma LLC.

Product NDC
70756-018
Status
Listed
Labeler
Lifestar Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215880
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70756-018 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70756-018-5170756001851500 TABLET in 1 BOTTLE (70756-018-51)
70756-018-907075600189090 TABLET in 1 BOTTLE (70756-018-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0502f935-af7a-4f1e-8c3e-29e20647c885

Use it

Look up 70756-018 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70756-018 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70756-018. 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.