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NDC 79903-112, Omeprazole magnesium, capsule, delayed release, from WALMART INC..

Product NDC
79903-112
Status
Listed
Labeler
WALMART INC.
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/79903-112 \
  -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
79903-112-14799030112141 BOTTLE in 1 CARTON (79903-112-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
79903-112-28799030112282 BOTTLE in 1 CARTON (79903-112-28) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
79903-112-42799030112423 BOTTLE in 1 CARTON (79903-112-42) / 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 79903-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/79903-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 79903-112. 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.