omeprazole and sodium bicarbonate (41250-938)

Drug Facts

Product Profile

Brand Name omeprazole and sodium bicarbonate

Generic Name omeprazole, sodium bicarbonate

Labeler meijer distribution inc

Dosage Form CAPSULE, GELATIN COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

Meijer Distribution Inc

Identifiers & Regulatory

Product NDC 41250-938

Product ID 41250-938_38a77306-7ef0-4938-9486-d327e25a0462

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA201361

Listing Expiration 2026-12-31

Marketing Start 2020-04-03

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 41250938

Hyphenated Format 41250-938

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 (41250-938-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE (41250-938-01)

source: ndc

Packages (1)

41250-938-03 3 BOTTLE in 1 CARTON (41250-938-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE (41250-938-01)

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": "38a77306-7ef0-4938-9486-d327e25a0462", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539"], "spl_set_id": ["bb7c1c5d-b915-42f5-a5a2-5f61b088028d"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (41250-938-03)  / 14 CAPSULE, GELATIN COATED in 1 BOTTLE (41250-938-01)", "package_ndc": "41250-938-03", "marketing_start_date": "20200403"}], "brand_name": "omeprazole and sodium bicarbonate", "product_id": "41250-938_38a77306-7ef0-4938-9486-d327e25a0462", "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": "41250-938", "generic_name": "Omeprazole, sodium bicarbonate", "labeler_name": "Meijer Distribution Inc", "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": "20200403", "listing_expiration_date": "20261231"}