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Omeprazole Magnesium

NDC 68016-760, Omeprazole Magnesium, capsule, delayed release, from Chain Drug Consortium, LLC.

Product NDC
68016-760
Status
Listed
Labeler
Chain Drug Consortium, LLC
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA078878
DEA schedule
None
Request
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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
68016-760-14680160760141 BOTTLE in 1 CARTON (68016-760-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
68016-760-28680160760282 BOTTLE in 1 CARTON (68016-760-28) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
68016-760-42680160760423 BOTTLE in 1 CARTON (68016-760-42) / 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 68016-760 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68016-760 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68016-760. 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.