Package 64980-676-09

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 64980-676-09
Digits Only 6498067609
Product NDC 64980-676
Product ID 64980-676_9fe81197-8014-4967-aa15-7525509d532c
Description

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

Marketing

Marketing Status
Marketed Since 2025-03-12
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

PANTOPRAZOLE SODIUM ndc-match (0.95)

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"}