omeprazole

Generic: omeprazole

Labeler: albertsons companies
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name omeprazole
Generic Name omeprazole
Labeler albertsons companies
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

omeprazole 20 mg/1

Manufacturer
Albertsons Companies

Identifiers & Regulatory

Product NDC 21130-018
Product ID 21130-018_53360ff9-d407-c729-dd32-2795bc8b40c1
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207740
Listing Expiration 2026-12-31
Marketing Start 2018-11-06

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 21130018
Hyphenated Format 21130-018

Supplemental Identifiers

RxCUI
402014
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 ANDA207740 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (21130-018-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (21130-018-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
  • 3 BOTTLE in 1 CARTON (21130-018-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
source: ndc

Packages (3)

21130-018-14 1 BOTTLE in 1 CARTON (21130-018-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE 21130-018-28 2 BOTTLE in 1 CARTON (21130-018-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE 21130-018-42 3 BOTTLE in 1 CARTON (21130-018-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

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": "53360ff9-d407-c729-dd32-2795bc8b40c1", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["402014"], "spl_set_id": ["249556e1-60d2-b0a1-c125-90c28fd4e7bd"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Albertsons Companies"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-018-14)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "21130-018-14", "marketing_start_date": "20230915"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (21130-018-28)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "21130-018-28", "marketing_start_date": "20230915"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (21130-018-42)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "21130-018-42", "marketing_start_date": "20230915"}], "brand_name": "Omeprazole", "product_id": "21130-018_53360ff9-d407-c729-dd32-2795bc8b40c1", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "21130-018", "generic_name": "Omeprazole", "labeler_name": "Albertsons Companies", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA207740", "marketing_category": "ANDA", "marketing_start_date": "20181106", "listing_expiration_date": "20261231"}