omeprazole

Generic: omeprazole

Labeler: walmart inc. (see also equate)
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name omeprazole
Generic Name omeprazole
Labeler walmart inc. (see also equate)
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

omeprazole magnesium 20.6 mg/1

Manufacturer
WALMART INC. (see also Equate)

Identifiers & Regulatory

Product NDC 79903-377
Product ID 79903-377_525b880b-439d-436f-95a4-cb155ae85679
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206582
Listing Expiration 2026-12-31
Marketing Start 2025-04-30

Pharmacologic Class

Classes
cytochrome p450 2c19 inhibitors [moa] proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79903377
Hyphenated Format 79903-377

Supplemental Identifiers

RxCUI
402014
UPC
0194346206292
UNII
426QFE7XLK

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 (source: ndc)
Generic Name omeprazole (source: ndc)
Application Number ANDA206582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20.6 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (79903-377-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
  • 3 BOTTLE, PLASTIC in 1 BOX (79903-377-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

79903-377-14 1 BOTTLE, PLASTIC in 1 BOX (79903-377-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 79903-377-42 3 BOTTLE, PLASTIC in 1 BOX (79903-377-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

Ingredients (1)

omeprazole magnesium (20.6 mg/1)

Linked Drug Pages (1)

Omeprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "525b880b-439d-436f-95a4-cb155ae85679", "openfda": {"upc": ["0194346206292"], "unii": ["426QFE7XLK"], "rxcui": ["402014"], "spl_set_id": ["d3c1ba08-680d-4e39-875c-1f1d42ae787c"], "manufacturer_name": ["WALMART INC. (see also Equate)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (79903-377-14)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "79903-377-14", "marketing_start_date": "20250430"}, {"sample": false, "description": "3 BOTTLE, PLASTIC in 1 BOX (79903-377-42)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "79903-377-42", "marketing_start_date": "20250430"}], "brand_name": "Omeprazole", "product_id": "79903-377_525b880b-439d-436f-95a4-cb155ae85679", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "79903-377", "generic_name": "Omeprazole", "labeler_name": "WALMART INC. (see also Equate)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20.6 mg/1"}], "application_number": "ANDA206582", "marketing_category": "ANDA", "marketing_start_date": "20250430", "listing_expiration_date": "20261231"}