pantoprazole sodium

Generic: pantoprazole

Labeler: xlcare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pantoprazole sodium 40 mg/1

Manufacturer
XLCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72865-230
Product ID 72865-230_f26fc428-a419-1008-e053-2a95a90a83fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202882
Listing Expiration 2026-12-31
Marketing Start 2022-05-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865230
Hyphenated Format 72865-230

Supplemental Identifiers

RxCUI
251872 314200
UPC
0372865230107
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 (source: ndc)
Application Number ANDA202882 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)
source: ndc

Packages (2)

72865-230-10 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10) 72865-230-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)

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": "f26fc428-a419-1008-e053-2a95a90a83fc", "openfda": {"upc": ["0372865230107"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["17468dbf-84b6-4c53-9ad5-341350d2cfab"], "manufacturer_name": ["XLCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)", "package_ndc": "72865-230-10", "marketing_start_date": "20220501"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)", "package_ndc": "72865-230-90", "marketing_start_date": "20220501"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "72865-230_f26fc428-a419-1008-e053-2a95a90a83fc", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72865-230", "generic_name": "PANTOPRAZOLE", "labeler_name": "XLCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20220501", "listing_expiration_date": "20261231"}