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OMEPRAZOLE

NDC 21130-783, Omeprazole, capsule, delayed release, from Safeway.

Product NDC
21130-783
Status
Listed
Labeler
Safeway
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA216096
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/21130-783 \
  -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
21130-783-01211300783011 BOTTLE in 1 CARTON (21130-783-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
21130-783-03211300783033 BOTTLE in 1 CARTON (21130-783-03) / 14 CAPSULE, 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 21130-783 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/21130-783 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 21130-783. 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.