Package 85509-1636-9

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 85509-1636-9
Digits Only 8550916369
Product NDC 85509-1636
Product ID 85509-1636_440b9278-eab8-6434-e063-6394a90ac398
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1636-9)

Marketing

Marketing Status
Marketed Since 2025-11-20
Brand pantoprazole sodium
Generic pantoprazole
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": "440b9278-eab8-6434-e063-6394a90ac398", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["440b9ae8-2fb8-5d35-e063-6294a90a82b6"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1636-3)", "package_ndc": "85509-1636-3", "marketing_start_date": "20251120"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1636-6)", "package_ndc": "85509-1636-6", "marketing_start_date": "20251120"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1636-9)", "package_ndc": "85509-1636-9", "marketing_start_date": "20251120"}], "brand_name": "Pantoprazole Sodium", "product_id": "85509-1636_440b9278-eab8-6434-e063-6394a90ac398", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "85509-1636", "generic_name": "Pantoprazole", "labeler_name": "PHOENIX RX 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"}