Package 55111-333-81
Brand: pantoprazole
Generic: pantoprazolePackage Facts
Identity
Package NDC
55111-333-81
Digits Only
5511133381
Product NDC
55111-333
Description
3 BLISTER PACK in 1 CARTON (55111-333-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)
Marketing
Marketing Status
Brand
pantoprazole
Generic
pantoprazole
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5c22ca2e-52db-fb09-be54-ddf8c4e428c8", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["564709e8-358f-c185-4ecb-b3849c3fe59c"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-01)", "package_ndc": "55111-333-01", "marketing_start_date": "20110119"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-05)", "package_ndc": "55111-333-05", "marketing_start_date": "20110119"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-10)", "package_ndc": "55111-333-10", "marketing_start_date": "20110119"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-30)", "package_ndc": "55111-333-30", "marketing_start_date": "20110119"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-333-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)", "package_ndc": "55111-333-78", "marketing_start_date": "20110119"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (55111-333-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)", "package_ndc": "55111-333-81", "marketing_start_date": "20110119"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-90)", "package_ndc": "55111-333-90", "marketing_start_date": "20110119"}], "brand_name": "Pantoprazole", "product_id": "55111-333_5c22ca2e-52db-fb09-be54-ddf8c4e428c8", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "55111-333", "generic_name": "Pantoprazole", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA077619", "marketing_category": "ANDA", "marketing_start_date": "20110119", "listing_expiration_date": "20261231"}