pantoprazole sodium dr

Generic: pantoprazole sodium dr

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium dr
Generic Name pantoprazole sodium dr
Labeler direct_rx
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-514
Product ID 72189-514_4c4adb93-e6cf-6f33-e063-6294a90a063b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202882
Listing Expiration 2027-12-31
Marketing Start 2023-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189514
Hyphenated Format 72189-514

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 dr (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 (72189-514-30)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-90)
source: ndc

Packages (2)

72189-514-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-30) 72189-514-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-90)

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 
{"route": ["ORAL"], "spl_id": "4c4adb93-e6cf-6f33-e063-6294a90a063b", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["0515ceaa-7d17-c92f-e063-6294a90a044e"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-30)", "package_ndc": "72189-514-30", "marketing_start_date": "20230911"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-90)", "package_ndc": "72189-514-90", "marketing_start_date": "20230911"}], "brand_name": "Pantoprazole Sodium DR", "product_id": "72189-514_4c4adb93-e6cf-6f33-e063-6294a90a063b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-514", "generic_name": "Pantoprazole Sodium DR", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium DR", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20271231"}