Package 71610-659-42

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 71610-659-42
Digits Only 7161065942
Product NDC 71610-659
Product ID 71610-659_269544ac-1dea-4047-87e6-6e04ff951b55
Description

1800 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-42)

Marketing

Marketing Status
Marketed Since 2023-02-17
Brand pantoprazole sodium
Generic pantoprazole
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": "269544ac-1dea-4047-87e6-6e04ff951b55", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["c10e9c12-e39d-4b0b-bd4c-10d3e9a4cf34"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-09)", "package_ndc": "71610-659-09", "marketing_start_date": "20220825"}, {"sample": false, "description": "1800 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-42)", "package_ndc": "71610-659-42", "marketing_start_date": "20230217"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "71610-659_269544ac-1dea-4047-87e6-6e04ff951b55", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71610-659", "generic_name": "PANTOPRAZOLE", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20220501", "listing_expiration_date": "20261231"}