pantoprazole sodium dr (80425-0085)

Drug Facts

Product Profile

Brand Name pantoprazole sodium dr

Generic Name pantoprazole sodium

Labeler advanced rx of tennessee, llc

Dosage Form TABLET, DELAYED RELEASE

Routes

ORAL

Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer

Advanced Rx of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0085

Product ID 80425-0085_2a98ff70-0367-7169-e063-6394a90adc74

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA205119

Listing Expiration 2026-12-31

Marketing Start 2016-06-20

Pharmacologic Class

Classes

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250085

Hyphenated Format 80425-0085

Supplemental Identifiers

RxCUI

251872

UNII

6871619Q5X

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 dr (source: ndc)

Generic Name pantoprazole sodium (source: ndc)

Application Number ANDA205119 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

20 mg/1

source: ndc

Packaging

90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3)

source: ndc

Packages (1)

80425-0085-3 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3)

Ingredients (1)

pantoprazole sodium (20 mg/1)

Linked Drug Pages (1)

Pantoprazole Sodium DR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "2a98ff70-0367-7169-e063-6394a90adc74", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["b3277cb8-26d0-bce0-e053-2a95a90af6dd"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3)", "package_ndc": "80425-0085-3", "marketing_start_date": "20160620"}], "brand_name": "Pantoprazole Sodium DR", "product_id": "80425-0085_2a98ff70-0367-7169-e063-6394a90adc74", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80425-0085", "generic_name": "Pantoprazole Sodium", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "brand_name_suffix": "DR", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA205119", "marketing_category": "ANDA", "marketing_start_date": "20160620", "listing_expiration_date": "20261231"}