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Omeprazole and Sodium Bicarbonate

NDC 75907-138, Omeprazole and Sodium Bicarbonate, powder, for suspension, from Dr. Reddy's Laboratories Inc.,.

Product NDC
75907-138
Status
Listed
Labeler
Dr. Reddy's Laboratories Inc.,
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA217784
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/75907-138 \
  -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
75907-138-427590701384242 PACKET in 1 CARTON (75907-138-42) / 1 POWDER, FOR SUSPENSION in 1 PACKET

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 75907-138 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/75907-138 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 75907-138. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.