omeprazole and sodium bicarbonate

Generic: omeprazole and sodium bicarbonate

Labeler: sciegen pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name omeprazole and sodium bicarbonate
Generic Name omeprazole and sodium bicarbonate
Labeler sciegen pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

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

Manufacturer
ScieGen Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 50228-363
Product ID 50228-363_25403f99-6570-5b4b-e063-6294a90a9963
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207476
Listing Expiration 2026-12-31
Marketing Start 2016-12-06

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 50228363
Hyphenated Format 50228-363

Supplemental Identifiers

RxCUI
616539 616541
UPC
0350228364300 0350228363303
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 and sodium bicarbonate (source: ndc)
Application Number ANDA207476 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 1100 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE (50228-363-05)
  • 30 CAPSULE in 1 BOTTLE (50228-363-30)
source: ndc

Packages (2)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "25403f99-6570-5b4b-e063-6294a90a9963", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "upc": ["0350228364300", "0350228363303"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539", "616541"], "spl_set_id": ["a107804e-b308-4e79-9447-07d93016f70f"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (50228-363-05)", "package_ndc": "50228-363-05", "marketing_start_date": "20161206"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50228-363-30)", "package_ndc": "50228-363-30", "marketing_start_date": "20161206"}], "brand_name": "Omeprazole and Sodium Bicarbonate", "product_id": "50228-363_25403f99-6570-5b4b-e063-6294a90a9963", "dosage_form": "CAPSULE", "pharm_class": ["Alkalinizing Activity [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50228-363", "generic_name": "Omeprazole and Sodium Bicarbonate", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION 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": "ANDA207476", "marketing_category": "ANDA", "marketing_start_date": "20161206", "listing_expiration_date": "20261231"}