pantoprazole sodium

Generic: pantoprazole sodium

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler rising pharma holdings, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-676
Product ID 64980-676_9fe81197-8014-4967-aa15-7525509d532c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219087
Listing Expiration 2026-12-31
Marketing Start 2025-03-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64980676
Hyphenated Format 64980-676

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 sodium (source: ndc)
Generic Name pantoprazole sodium (source: ndc)
Application Number ANDA219087 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (64980-676-09)
source: ndc

Packages (1)

64980-676-09 90 TABLET, DELAYED RELEASE in 1 BOTTLE (64980-676-09)

Ingredients (1)

pantoprazole sodium (20 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": "9fe81197-8014-4967-aa15-7525509d532c", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["91a6b13f-457f-4136-9541-c4adb9c3c35c"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (64980-676-09)", "package_ndc": "64980-676-09", "marketing_start_date": "20250312"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "64980-676_9fe81197-8014-4967-aa15-7525509d532c", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "64980-676", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA219087", "marketing_category": "ANDA", "marketing_start_date": "20250312", "listing_expiration_date": "20261231"}