omeprazole and sodium bicarbonate
Generic: omeprazole, sodium bicarbonate
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
omeprazole and sodium bicarbonate
Generic Name
omeprazole, sodium bicarbonate
Labeler
cvs pharmacy
Dosage Form
CAPSULE, GELATIN COATED
Routes
Active Ingredients
omeprazole 20 mg/1, sodium bicarbonate 1100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59779-732
Product ID
59779-732_a6fecbac-6464-4363-98b8-700b37d8647f
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA201361
Listing Expiration
2026-12-31
Marketing Start
2016-07-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59779732
Hyphenated Format
59779-732
Supplemental Identifiers
RxCUI
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, sodium bicarbonate (source: ndc)
Application Number
ANDA201361 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
- 1100 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (59779-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE
- 3 BOTTLE in 1 CARTON (59779-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a6fecbac-6464-4363-98b8-700b37d8647f", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539"], "spl_set_id": ["186732a3-13b9-4ea2-ba54-424f63298a2e"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59779-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE", "package_ndc": "59779-732-01", "marketing_start_date": "20160715"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (59779-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE", "package_ndc": "59779-732-03", "marketing_start_date": "20160715"}], "brand_name": "Omeprazole and Sodium Bicarbonate", "product_id": "59779-732_a6fecbac-6464-4363-98b8-700b37d8647f", "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": "59779-732", "generic_name": "Omeprazole, sodium bicarbonate", "labeler_name": "CVS Pharmacy", "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": "20160715", "listing_expiration_date": "20261231"}