acid reducer

Generic: esomeprazole magnesium

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acid reducer
Generic Name esomeprazole magnesium
Labeler p & l development, llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

esomeprazole magnesium 20 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-056
Product ID 59726-056_03fda90d-5e9e-4340-899b-0e3734510a66
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA212088
Marketing Start 2020-12-31
Marketing End 2026-06-30

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 59726056
Hyphenated Format 59726-056

Supplemental Identifiers

RxCUI
433733
UNII
R6DXU4WAY9

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 esomeprazole magnesium (source: ndc)
Application Number ANDA212088 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (59726-056-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
  • 3 BOTTLE, PLASTIC in 1 CARTON (59726-056-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

Ingredients (1)

esomeprazole magnesium (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "03fda90d-5e9e-4340-899b-0e3734510a66", "openfda": {"unii": ["R6DXU4WAY9"], "rxcui": ["433733"], "spl_set_id": ["08f09939-10d1-4380-81bb-826856444674"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59726-056-14)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "59726-056-14", "marketing_end_date": "20260630", "marketing_start_date": "20201231"}, {"sample": false, "description": "3 BOTTLE, PLASTIC in 1 CARTON (59726-056-42)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "59726-056-42", "marketing_end_date": "20260630", "marketing_start_date": "20201231"}], "brand_name": "Acid Reducer", "product_id": "59726-056_03fda90d-5e9e-4340-899b-0e3734510a66", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "59726-056", "generic_name": "Esomeprazole magnesium", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acid Reducer", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA212088", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20201231"}