omeprazole and sodium bicarbonate

Generic: omeprazole, sodium bicarbonate

Labeler: oceanside pharmaceuticals
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 oceanside pharmaceuticals
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

omeprazole 20 mg/1, sodium bicarbonate 1680 mg/1

Manufacturer
Oceanside Pharmaceuticals

Identifiers & Regulatory

Product NDC 68682-990
Product ID 68682-990_342c0d17-867e-d8da-e063-6394a90a3151
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021636
Marketing Start 2004-06-15
Marketing End 2026-08-31

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 68682990
Hyphenated Format 68682-990

Supplemental Identifiers

RxCUI
616539 616541 753557 753562
UPC
0368682102307 0368682104301
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 NDA021636 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 1680 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (68682-990-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
source: ndc

Packages (1)

68682-990-30 30 PACKET in 1 CARTON (68682-990-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET

Ingredients (2)

omeprazole (20 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": "342c0d17-867e-d8da-e063-6394a90a3151", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "upc": ["0368682102307", "0368682104301"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539", "616541", "753557", "753562"], "spl_set_id": ["c26b6893-8264-4d4a-ac7e-1ddda933451e"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (68682-990-30)  / 1 POWDER, FOR SUSPENSION in 1 PACKET", "package_ndc": "68682-990-30", "marketing_end_date": "20260831", "marketing_start_date": "20040615"}], "brand_name": "Omeprazole and Sodium Bicarbonate", "product_id": "68682-990_342c0d17-867e-d8da-e063-6394a90a3151", "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": "68682-990", "generic_name": "omeprazole, sodium bicarbonate", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole and Sodium Bicarbonate", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1680 mg/1"}], "application_number": "NDA021636", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260831", "marketing_start_date": "20040615"}