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topcare omeprazole

NDC 76162-470, omeprazole, tablet, delayed release, from Topco Associates LLC.

Product NDC
76162-470
Status
Listed
Labeler
Topco Associates LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
NDA
Application
NDA022032
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76162-470 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OMEPRAZOLE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
76162-470-01761620470011 BOTTLE in 1 CARTON (76162-470-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
76162-470-03761620470033 BOTTLE in 1 CARTON (76162-470-03) / 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 76162-470 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76162-470 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76162-470. 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.