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Omeprazole 20 mg

NDC 25000-094, Omeprazole 20 mg, tablet, delayed release, from MARKSANS PHARMA LIMITED.

Product NDC
25000-094
Status
Listed
Labeler
MARKSANS PHARMA LIMITED
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA218829
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25000-094 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OMEPRAZOLE MAGNESIUM20 mg/1

Pharmacologic classes

Cytochrome P450 2C19 Inhibitors [MoA]; Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
25000-094-76250000094761 BOTTLE in 1 CARTON (25000-094-76) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
25000-094-81250000094811 BLISTER PACK in 1 CARTON (25000-094-81) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 25000-094 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25000-094 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25000-094. 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.