Package 59651-671-30

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 59651-671-30
Digits Only 5965167130
Product NDC 59651-671
Product ID 59651-671_b3cec41e-e98b-470a-8ba2-c31537023989
Description

30 PACKET in 1 CARTON (59651-671-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET

Marketing

Marketing Status
Marketed Since 2025-03-31
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": "b3cec41e-e98b-470a-8ba2-c31537023989", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["b3cec41e-e98b-470a-8ba2-c31537023989"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (59651-671-30)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET", "package_ndc": "59651-671-30", "marketing_start_date": "20250331"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "59651-671_b3cec41e-e98b-470a-8ba2-c31537023989", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "59651-671", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA217923", "marketing_category": "ANDA", "marketing_start_date": "20250331", "listing_expiration_date": "20261231"}