Package 50090-5379-0

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 50090-5379-0
Digits Only 5009053790
Product NDC 50090-5379
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5379-0)

Marketing

Marketing Status
Marketed Since 2020-11-19
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d22b2c34-cd1e-402a-9a15-707f7f3d52ed", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["485212d4-caee-4a55-8299-87a28d6bd8f0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5379-0)", "package_ndc": "50090-5379-0", "marketing_start_date": "20201119"}], "brand_name": "Pantoprazole Sodium", "product_id": "50090-5379_d22b2c34-cd1e-402a-9a15-707f7f3d52ed", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-5379", "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": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20261231"}