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Omeprazole Delayed-Release

NDC 37808-569, Omeprazole, tablet, delayed release, from H-E-B.

Product NDC
37808-569
Status
Listed
Labeler
H-E-B
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/37808-569 \
  -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
37808-569-41378080569413 BOTTLE in 1 CARTON (37808-569-41) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37808-569-45378080569451 BOTTLE in 1 CARTON (37808-569-45) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
37808-569-82378080569822 BOTTLE in 1 CARTON (37808-569-82) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

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 37808-569 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/37808-569 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 37808-569. 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.