omeprazole and sodium bicarbonate

Generic: omeprazole, sodium bicarbonate

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name omeprazole and sodium bicarbonate
Generic Name omeprazole, sodium bicarbonate
Labeler h e b
Dosage Form CAPSULE, GELATIN COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-732
Product ID 37808-732_99b31e8b-1cf3-47a5-b0f7-31e0530691ed
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA201361
Listing Expiration 2026-12-31
Marketing Start 2017-08-25

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 37808732
Hyphenated Format 37808-732

Supplemental Identifiers

RxCUI
616539
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 ANDA201361 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 1100 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (37808-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE
  • 3 BOTTLE in 1 CARTON (37808-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE
source: ndc

Packages (2)

37808-732-01 1 BOTTLE in 1 CARTON (37808-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE 37808-732-03 3 BOTTLE in 1 CARTON (37808-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLE

Ingredients (2)

omeprazole (20 mg/1) sodium bicarbonate (1100 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": "99b31e8b-1cf3-47a5-b0f7-31e0530691ed", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539"], "spl_set_id": ["ddc8d73f-f4a1-42a7-89ee-420346820f61"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-732-01)  / 14 CAPSULE, GELATIN COATED in 1 BOTTLE", "package_ndc": "37808-732-01", "marketing_start_date": "20170825"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (37808-732-03)  / 14 CAPSULE, GELATIN COATED in 1 BOTTLE", "package_ndc": "37808-732-03", "marketing_start_date": "20170825"}], "brand_name": "Omeprazole and sodium bicarbonate", "product_id": "37808-732_99b31e8b-1cf3-47a5-b0f7-31e0530691ed", "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": "37808-732", "generic_name": "Omeprazole, sodium bicarbonate", "labeler_name": "H E B", "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": "20170825", "listing_expiration_date": "20261231"}