esomeprazole magnesium

Generic: esomeprazole magnesium

Labeler: zhejiang yongtai pharmaceutical co., ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name esomeprazole magnesium
Generic Name esomeprazole magnesium
Labeler zhejiang yongtai pharmaceutical co., ltd
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

esomeprazole magnesium 20 mg/1

Manufacturer
Zhejiang Yongtai Pharmaceutical Co., Ltd

Identifiers & Regulatory

Product NDC 69434-012
Product ID 69434-012_e9332607-e8e1-4b84-884a-7ae2b4313fb7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217022
Listing Expiration 2026-12-31
Marketing Start 2025-01-09

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 69434012
Hyphenated Format 69434-012

Supplemental Identifiers

RxCUI
606726 606730
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 esomeprazole magnesium (source: ndc)
Generic Name esomeprazole magnesium (source: ndc)
Application Number ANDA217022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-01)
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-02)
  • 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-03)
source: ndc

Packages (3)

69434-012-01 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-01) 69434-012-02 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-02) 69434-012-03 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-03)

Ingredients (1)

esomeprazole magnesium (20 mg/1)

Linked Drug Pages (1)

Esomeprazole magnesium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e9332607-e8e1-4b84-884a-7ae2b4313fb7", "openfda": {"unii": ["R6DXU4WAY9"], "rxcui": ["606726", "606730"], "spl_set_id": ["5ea93b2b-115b-4591-97ea-311d77e3a5ba"], "manufacturer_name": ["Zhejiang Yongtai Pharmaceutical Co., Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-01)", "package_ndc": "69434-012-01", "marketing_start_date": "20250109"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-02)", "package_ndc": "69434-012-02", "marketing_start_date": "20250109"}, {"sample": false, "description": "500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69434-012-03)", "package_ndc": "69434-012-03", "marketing_start_date": "20250109"}], "brand_name": "Esomeprazole magnesium", "product_id": "69434-012_e9332607-e8e1-4b84-884a-7ae2b4313fb7", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "69434-012", "generic_name": "Esomeprazole magnesium", "labeler_name": "Zhejiang Yongtai Pharmaceutical Co., Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Esomeprazole magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA217022", "marketing_category": "ANDA", "marketing_start_date": "20250109", "listing_expiration_date": "20261231"}