pantoprazole sodium

Generic: pantoprazole sodium

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

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler lannett company, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 62175-617
Product ID 62175-617_cfbf12d8-f656-4b99-bd2e-fb11bab669e5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078281
Listing Expiration 2026-12-31
Marketing Start 2011-01-20

Pharmacologic Class

Classes
proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62175617
Hyphenated Format 62175-617

Supplemental Identifiers

RxCUI
251872 314200
UPC
0362175617460 0362175180469
UNII
6871619Q5X

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 pantoprazole sodium (source: ndc)
Generic Name pantoprazole sodium (source: ndc)
Application Number ANDA078281 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-43)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-46)
source: ndc

Packages (2)

62175-617-43 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-43) 62175-617-46 90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-46)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Pantoprazole Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cfbf12d8-f656-4b99-bd2e-fb11bab669e5", "openfda": {"upc": ["0362175617460", "0362175180469"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["e7705bf6-e473-4b9c-bb5d-57e26ffe7b97"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-43)", "package_ndc": "62175-617-43", "marketing_start_date": "20110120"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-617-46)", "package_ndc": "62175-617-46", "marketing_start_date": "20110120"}], "brand_name": "Pantoprazole Sodium", "product_id": "62175-617_cfbf12d8-f656-4b99-bd2e-fb11bab669e5", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62175-617", "generic_name": "Pantoprazole Sodium", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA078281", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}