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Omeprazole and Sodium Bicarbonate

NDC 70954-798, Omeprazole and Sodium Bicarbonate, powder, for suspension, from ANI Pharmaceuticals, Inc..

Product NDC
70954-798
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219161
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-798 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OMEPRAZOLE40 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
70954-798-207095407982030 PACKET in 1 CARTON (70954-798-20) / 1 POWDER, FOR SUSPENSION in 1 PACKET (70954-798-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/63c3bd6c-a586-4ec0-8f45-ed936936dfeb

  • NADAC price for package 70954079820

    GET /v1/drugs/nadac/70954079820

Use it

Look up 70954-798 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-798 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-798. 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.