pantoprazole sodium dr (80425-0162)

Drug Facts

Product Profile

Brand Name pantoprazole sodium dr

Generic Name pantoprazole sodium

Labeler advanced rx pharmacy of tennessee, llc

Dosage Form TABLET, DELAYED RELEASE

Routes

ORAL

Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer

Advanced Rx Pharmacy of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0162

Product ID 80425-0162_2a99a670-af2e-299d-e063-6294a90a05d2

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA202882

Listing Expiration 2026-12-31

Marketing Start 2014-09-10

Pharmacologic Class

Classes

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250162

Hyphenated Format 80425-0162

Supplemental Identifiers

RxCUI

314200

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 ANDA202882 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

40 mg/1

source: ndc

Packaging

30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-1)
60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-2)
90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-3)

source: ndc

Packages (3)

80425-0162-1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-1) 80425-0162-2 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-2) 80425-0162-3 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-3)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Pantoprazole Sodium DR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

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