Package 35573-428-80
Brand: pantoprazole sodium
Generic: pantoprazole sodiumPackage Facts
Identity
Package NDC
35573-428-80
Digits Only
3557342880
Product NDC
35573-428
Description
10 BLISTER PACK in 1 CARTON (35573-428-80) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Marketing
Marketing Status
Brand
pantoprazole sodium
Generic
pantoprazole sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb46c38e-b217-4295-9569-98c16cad56df", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["3cc5197e-6b39-4415-b963-d4bbeecd7953"], "manufacturer_name": ["Burel Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (35573-428-80) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "35573-428-80", "marketing_start_date": "20200420"}], "brand_name": "Pantoprazole Sodium", "product_id": "35573-428_eb46c38e-b217-4295-9569-98c16cad56df", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "35573-428", "generic_name": "Pantoprazole Sodium", "labeler_name": "Burel Pharmaceuticals, LLC", "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": "20200420", "listing_expiration_date": "20271231"}