omeprazole

Generic: omeprazole

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name omeprazole
Generic Name omeprazole
Labeler rite aid corporation
Dosage Form TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
Routes
ORAL
Active Ingredients

omeprazole 20 mg/1

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-1040
Product ID 11822-1040_0662e92e-ed7c-48e7-a7f6-7de0b60d06a8
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA209400
Listing Expiration 2026-12-31
Marketing Start 2018-03-29

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 118221040
Hyphenated Format 11822-1040

Supplemental Identifiers

RxCUI
2003656
UNII
KG60484QX9
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 (source: ndc)
Generic Name omeprazole (source: ndc)
Application Number NDA209400 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 3 CARTON in 1 CARTON (11822-1040-1) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
  • 14 BLISTER PACK in 1 CARTON (11822-1040-2) / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

11822-1040-1 3 CARTON in 1 CARTON (11822-1040-1) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK 11822-1040-2 14 BLISTER PACK in 1 CARTON (11822-1040-2) / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK

Ingredients (1)

omeprazole (20 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": "0662e92e-ed7c-48e7-a7f6-7de0b60d06a8", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["2003656"], "spl_set_id": ["6919399e-f112-4274-b4de-df0b4c391e63"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 CARTON in 1 CARTON (11822-1040-1)  / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-1040-1", "marketing_start_date": "20180329"}, {"sample": false, "description": "14 BLISTER PACK in 1 CARTON (11822-1040-2)  / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-1040-2", "marketing_start_date": "20190313"}], "brand_name": "omeprazole", "product_id": "11822-1040_0662e92e-ed7c-48e7-a7f6-7de0b60d06a8", "dosage_form": "TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "11822-1040", "generic_name": "omeprazole", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "NDA209400", "marketing_category": "NDA", "marketing_start_date": "20180329", "listing_expiration_date": "20261231"}