omeprazole and sodium bicarbonate

Generic: omeprazole and sodium bicarbonate

Labeler: phoenix rx llc
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 phoenix rx llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

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

Manufacturer
PHOENIX RX LLC

Identifiers & Regulatory

Product NDC 85509-1031
Product ID 85509-1031_3b2bf542-9d8a-6ff6-e063-6394a90a3fae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204228
Listing Expiration 2026-12-31
Marketing Start 2016-07-15

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 855091031
Hyphenated Format 85509-1031

Supplemental Identifiers

RxCUI
616539
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 and sodium bicarbonate (source: ndc)
Application Number ANDA204228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 1100 mg/1
source: ndc
Packaging
  • 15 CAPSULE in 1 BOTTLE (85509-1031-1)
  • 30 CAPSULE in 1 BOTTLE (85509-1031-3)
  • 60 CAPSULE in 1 BOTTLE (85509-1031-6)
source: ndc

Packages (3)

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": "3b2bf542-9d8a-6ff6-e063-6394a90a3fae", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539"], "spl_set_id": ["3b2bf501-fd81-6ffa-e063-6394a90afe42"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 CAPSULE in 1 BOTTLE (85509-1031-1)", "package_ndc": "85509-1031-1", "marketing_start_date": "20250730"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (85509-1031-3)", "package_ndc": "85509-1031-3", "marketing_start_date": "20250730"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (85509-1031-6)", "package_ndc": "85509-1031-6", "marketing_start_date": "20250730"}], "brand_name": "Omeprazole and Sodium Bicarbonate", "product_id": "85509-1031_3b2bf542-9d8a-6ff6-e063-6394a90a3fae", "dosage_form": "CAPSULE", "pharm_class": ["Alkalinizing Activity [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "85509-1031", "generic_name": "Omeprazole and Sodium Bicarbonate", "labeler_name": "PHOENIX RX LLC", "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": "ANDA204228", "marketing_category": "ANDA", "marketing_start_date": "20160715", "listing_expiration_date": "20261231"}