acid reducer

Generic: omeprazole

Labeler: northeast pharma
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acid reducer
Generic Name omeprazole
Labeler northeast pharma
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

omeprazole magnesium 20 mg/1

Manufacturer
NORTHEAST PHARMA

Identifiers & Regulatory

Product NDC 80136-852
Product ID 80136-852_29498c01-1121-44bf-9a93-d5c5438bb83c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206877
Listing Expiration 2026-12-31
Marketing Start 2021-07-05

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 80136852
Hyphenated Format 80136-852

Supplemental Identifiers

RxCUI
402014
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 acid reducer (source: ndc)
Generic Name omeprazole (source: ndc)
Application Number ANDA206877 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 3 BOTTLE in 1 CARTON (80136-852-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
  • 3 BLISTER PACK in 1 CARTON (80136-852-42) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

80136-852-03 3 BOTTLE in 1 CARTON (80136-852-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE 80136-852-42 3 BLISTER PACK in 1 CARTON (80136-852-42) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Ingredients (1)

omeprazole magnesium (20 mg/1)

Linked Drug Pages (1)

Acid Reducer ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "29498c01-1121-44bf-9a93-d5c5438bb83c", "openfda": {"unii": ["426QFE7XLK"], "rxcui": ["402014"], "spl_set_id": ["35ceccb5-dc3d-4ee1-bdac-35cb52c22f59"], "manufacturer_name": ["NORTHEAST PHARMA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (80136-852-03)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "80136-852-03", "marketing_start_date": "20210705"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (80136-852-42)  / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "80136-852-42", "marketing_start_date": "20220113"}], "brand_name": "Acid Reducer", "product_id": "80136-852_29498c01-1121-44bf-9a93-d5c5438bb83c", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80136-852", "generic_name": "Omeprazole", "labeler_name": "NORTHEAST PHARMA", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acid Reducer", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA206877", "marketing_category": "ANDA", "marketing_start_date": "20210705", "listing_expiration_date": "20261231"}