Package 51655-075-25

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 51655-075-25
Digits Only 5165507525
Product NDC 51655-075
Product ID 51655-075_499cdde9-4c46-def9-e063-6394a90a9788
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-25)

Marketing

Marketing Status
Marketed Since 2024-02-23
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": "499cdde9-4c46-def9-e063-6394a90a9788", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["f2a1af50-a051-3e55-e053-2a95a90a9184"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-25)", "package_ndc": "51655-075-25", "marketing_start_date": "20240223"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-52)", "package_ndc": "51655-075-52", "marketing_start_date": "20220927"}], "brand_name": "Pantoprazole Sodium", "product_id": "51655-075_499cdde9-4c46-def9-e063-6394a90a9788", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "51655-075", "generic_name": "Pantoprazole Sodium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20220927", "listing_expiration_date": "20271231"}