omeprazole and sodium bicarbonate
Generic: omeprazole and sodium bicarbonate
Labeler: sciegen pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
omeprazole and sodium bicarbonate
Generic Name
omeprazole and sodium bicarbonate
Labeler
sciegen pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
omeprazole 20 mg/1, sodium bicarbonate 1100 mg/1
Manufacturer
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50228363
Hyphenated Format
50228-363
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 20 mg/1
- 1100 mg/1
Packaging
- 500 CAPSULE in 1 BOTTLE (50228-363-05)
- 30 CAPSULE in 1 BOTTLE (50228-363-30)
Packages (2)
Ingredients (2)
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"}