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Omeprazole

NDC 79903-377, Omeprazole, tablet, delayed release, from WALMART INC. (see also Equate).

Product NDC
79903-377
Status
Listed
Labeler
WALMART INC. (see also Equate)
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA206582
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/79903-377 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OMEPRAZOLE MAGNESIUM20.6 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
79903-377-14799030377141 BOTTLE, PLASTIC in 1 BOX (79903-377-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
79903-377-42799030377423 BOTTLE, PLASTIC in 1 BOX (79903-377-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

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 79903-377 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/79903-377 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 79903-377. 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.