Package 50090-5794-1

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 50090-5794-1
Digits Only 5009057941
Product NDC 50090-5794
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-1)

Marketing

Marketing Status
Marketed Since 2021-10-11
Brand pantoprazole sodium
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e3af5aa-2ecf-42b3-944e-ce46273f8349", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["3a8fa326-ad75-4b6d-8832-0a2357eeca2f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-0)", "package_ndc": "50090-5794-0", "marketing_start_date": "20211011"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-1)", "package_ndc": "50090-5794-1", "marketing_start_date": "20211011"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "50090-5794_2e3af5aa-2ecf-42b3-944e-ce46273f8349", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-5794", "generic_name": "PANTOPRAZOLE", "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": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}