pantoprazole

Generic: pantoprazole

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole
Generic Name pantoprazole
Labeler northstar rxllc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-177
Product ID 72603-177_57338853-6995-de1e-62ca-be5505c8d656
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077619
Listing Expiration 2026-12-31
Marketing Start 2023-12-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603177
Hyphenated Format 72603-177

Supplemental Identifiers

RxCUI
251872 314200
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 (source: ndc)
Generic Name pantoprazole (source: ndc)
Application Number ANDA077619 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-177-01)
source: ndc

Packages (1)

72603-177-01 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-177-01)

Ingredients (1)

pantoprazole sodium (20 mg/1)

Linked Drug Pages (1)

Pantoprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "57338853-6995-de1e-62ca-be5505c8d656", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["82f0103a-2b97-d210-6d7d-c627d60ad694"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-177-01)", "package_ndc": "72603-177-01", "marketing_start_date": "20231215"}], "brand_name": "Pantoprazole", "product_id": "72603-177_57338853-6995-de1e-62ca-be5505c8d656", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72603-177", "generic_name": "Pantoprazole", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077619", "marketing_category": "ANDA", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}