omeprazole and sodium bicarbonate (0363-0732)

Drug Facts

Product Profile

Brand Name omeprazole and sodium bicarbonate

Generic Name omeprazole, sodium bicarbonate

Labeler walgreen company

Dosage Form CAPSULE, GELATIN COATED

Routes

ORAL

Active Ingredients

omeprazole 20 mg/1, sodium bicarbonate 1100 mg/1

Manufacturer

Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0732

Product ID 0363-0732_418a1ab3-af9c-459d-b8b3-471788d50d8d

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA201361

Listing Expiration 2026-12-31

Marketing Start 2016-07-15

Pharmacologic Class

Established (EPC)

proton pump inhibitor [epc]

Mechanism of Action

proton pump inhibitors [moa] cytochrome p450 2c19 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630732

Hyphenated Format 0363-0732

Supplemental Identifiers

RxCUI

616539

UNII

KG60484QX9 8MDF5V39QO

NUI

N0000175525 N0000000147 N0000182140

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name omeprazole and sodium bicarbonate (source: ndc)

Generic Name omeprazole, sodium bicarbonate (source: ndc)

Application Number ANDA201361 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

20 mg/1
1100 mg/1

source: ndc

Packaging

3 BOTTLE in 1 CARTON (0363-0732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE (0363-0732-01)

source: ndc

Packages (1)

0363-0732-03 3 BOTTLE in 1 CARTON (0363-0732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE (0363-0732-01)

Ingredients (2)

omeprazole (20 mg/1) sodium bicarbonate (1100 mg/1)

Linked Drug Pages (1)

Omeprazole and sodium bicarbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "418a1ab3-af9c-459d-b8b3-471788d50d8d", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539"], "spl_set_id": ["8753a131-f8b1-48e1-993b-73c1ee635fef"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (0363-0732-03)  / 14 CAPSULE, GELATIN COATED in 1 BOTTLE (0363-0732-01)", "package_ndc": "0363-0732-03", "marketing_start_date": "20160715"}], "brand_name": "Omeprazole and sodium bicarbonate", "product_id": "0363-0732_418a1ab3-af9c-459d-b8b3-471788d50d8d", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0363-0732", "generic_name": "Omeprazole, sodium bicarbonate", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Omeprazole and sodium bicarbonate", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1100 mg/1"}], "application_number": "ANDA201361", "marketing_category": "ANDA", "marketing_start_date": "20160715", "listing_expiration_date": "20261231"}