pantoprazole sodium

Generic: pantoprazole sodium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler bryant ranch prepack
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1746
Product ID 72162-1746_3e5421ef-0875-4a04-b17d-95cca0052c83
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 721621746
Hyphenated Format 72162-1746

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 (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
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-3)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-6)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-9)
source: ndc

Packages (3)

72162-1746-3 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-3) 72162-1746-6 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-6) 72162-1746-9 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-9)

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": "3e5421ef-0875-4a04-b17d-95cca0052c83", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["3e5421ef-0875-4a04-b17d-95cca0052c83"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-3)", "package_ndc": "72162-1746-3", "marketing_start_date": "20240404"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-6)", "package_ndc": "72162-1746-6", "marketing_start_date": "20240404"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-9)", "package_ndc": "72162-1746-9", "marketing_start_date": "20240404"}], "brand_name": "Pantoprazole Sodium", "product_id": "72162-1746_3e5421ef-0875-4a04-b17d-95cca0052c83", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72162-1746", "generic_name": "Pantoprazole Sodium", "labeler_name": "Bryant Ranch Prepack", "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"}