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NDC 68012-052, omeprazole and sodium bicarbonate, powder, for suspension, from Santarus, Inc...

Product NDC
68012-052
Status
Listed
Labeler
Santarus, Inc..
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021636
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68012-052 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OMEPRAZOLE20 mg/1
  • SODIUM BICARBONATE1680 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cd6868b9-5824-442b-8d65-4db29ecb70a4

Use it

Look up 68012-052 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68012-052 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68012-052. 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.