Package 50090-7512-0

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7512-0
Digits Only 5009075120
Product NDC 50090-7512
Product ID 50090-7512_a12b8b2c-799f-4090-81be-340ac97c6920
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7512-0)

Marketing

Marketing Status
Marketed Since 2025-03-10
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a12b8b2c-799f-4090-81be-340ac97c6920", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["81696241-17d5-4d35-9e59-8c28469ffd2c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7512-0)", "package_ndc": "50090-7512-0", "marketing_start_date": "20250310"}, {"sample": false, "description": "12960 TABLET, DELAYED RELEASE in 1 CASE (50090-7512-1)", "package_ndc": "50090-7512-1", "marketing_start_date": "20250310"}], "brand_name": "Pantoprazole Sodium", "product_id": "50090-7512_a12b8b2c-799f-4090-81be-340ac97c6920", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-7512", "generic_name": "Pantoprazole Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA090074", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}