Package 65162-636-03

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 65162-636-03
Digits Only 6516263603
Product NDC 65162-636
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-636-03)

Marketing

Marketing Status
Marketed Since 2016-06-20
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": "774b587f-7d77-4d2e-97f6-2b19d8cec56a", "openfda": {"upc": ["0365162637038"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["f3ded82a-cf0d-4844-944a-75f9f9215ff0"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-636-03)", "package_ndc": "65162-636-03", "marketing_start_date": "20160620"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-636-09)", "package_ndc": "65162-636-09", "marketing_start_date": "20160620"}], "brand_name": "Pantoprazole Sodium", "product_id": "65162-636_774b587f-7d77-4d2e-97f6-2b19d8cec56a", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "65162-636", "generic_name": "Pantoprazole", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA205119", "marketing_category": "ANDA", "marketing_start_date": "20160620", "listing_expiration_date": "20261231"}