omeprazole and sodium bicarbonate

Generic: omeprazole, sodium bicarbonate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name omeprazole and sodium bicarbonate
Generic Name omeprazole, sodium bicarbonate
Labeler bryant ranch prepack
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

omeprazole 40 mg/1, sodium bicarbonate 1680 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1907
Product ID 72162-1907_8a5c4c85-2e6b-4e66-a450-55885e8ae67e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021636
Marketing Start 2004-06-15
Marketing End 2026-04-30

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 721621907
Hyphenated Format 72162-1907

Supplemental Identifiers

RxCUI
753557
UNII
KG60484QX9 8MDF5V39QO
NUI
N0000175525 N0000000147 N0000182140

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 NDA021636 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
  • 1680 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (72162-1907-3) / 1 POWDER, FOR SUSPENSION in 1 PACKET
source: ndc

Packages (1)

72162-1907-3 30 PACKET in 1 CARTON (72162-1907-3) / 1 POWDER, FOR SUSPENSION in 1 PACKET

Ingredients (2)

omeprazole (40 mg/1) sodium bicarbonate (1680 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": "8a5c4c85-2e6b-4e66-a450-55885e8ae67e", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["753557"], "spl_set_id": ["8a5c4c85-2e6b-4e66-a450-55885e8ae67e"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (72162-1907-3)  / 1 POWDER, FOR SUSPENSION in 1 PACKET", "package_ndc": "72162-1907-3", "marketing_end_date": "20260430", "marketing_start_date": "20040615"}], "brand_name": "Omeprazole and Sodium Bicarbonate", "product_id": "72162-1907_8a5c4c85-2e6b-4e66-a450-55885e8ae67e", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Alkalinizing Activity [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72162-1907", "generic_name": "omeprazole, sodium bicarbonate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole and Sodium Bicarbonate", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "40 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1680 mg/1"}], "application_number": "NDA021636", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260430", "marketing_start_date": "20040615"}