esomeprazole magnesium

Generic: esomeprazole magnesium

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name esomeprazole magnesium
Generic Name esomeprazole magnesium
Labeler lannett company, inc.
Dosage Form CAPSULE, DELAYED RELEASE PELLETS
Routes
ORAL
Active Ingredients

esomeprazole magnesium 40 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 62175-840
Product ID 62175-840_c7191b9f-a102-4242-91b3-209713bfecf3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205563
Listing Expiration 2026-12-31
Marketing Start 2017-09-01

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 62175840
Hyphenated Format 62175-840

Supplemental Identifiers

RxCUI
606726 606730
UPC
0362175840325 0362175820327
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 ANDA205563 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-840-32)
  • 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-840-43)
  • 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-840-46)
source: ndc

Packages (3)

Ingredients (1)

esomeprazole magnesium (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c7191b9f-a102-4242-91b3-209713bfecf3", "openfda": {"upc": ["0362175840325", "0362175820327"], "unii": ["R6DXU4WAY9"], "rxcui": ["606726", "606730"], "spl_set_id": ["eb8f8b81-d482-4b94-be87-c766f49e753f"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-840-32)", "package_ndc": "62175-840-32", "marketing_start_date": "20170901"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-840-43)", "package_ndc": "62175-840-43", "marketing_start_date": "20170901"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-840-46)", "package_ndc": "62175-840-46", "marketing_start_date": "20170901"}], "brand_name": "Esomeprazole Magnesium", "product_id": "62175-840_c7191b9f-a102-4242-91b3-209713bfecf3", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62175-840", "generic_name": "Esomeprazole Magnesium", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Esomeprazole Magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "40 mg/1"}], "application_number": "ANDA205563", "marketing_category": "ANDA", "marketing_start_date": "20170901", "listing_expiration_date": "20261231"}