Package 60760-639-60
Brand: pantoprazole sodium
Generic: pantoprazole sodiumPackage Facts
Identity
Package NDC
60760-639-60
Digits Only
6076063960
Product NDC
60760-639
Description
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-639-60)
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": "e39f41ed-0903-9f0e-e053-2995a90ab36a", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["e39f41ed-0902-9f0e-e053-2995a90ab36a"], "manufacturer_name": ["St Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-639-60)", "package_ndc": "60760-639-60", "marketing_start_date": "20220622"}], "brand_name": "Pantoprazole Sodium", "product_id": "60760-639_e39f41ed-0903-9f0e-e053-2995a90ab36a", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "60760-639", "generic_name": "Pantoprazole Sodium", "labeler_name": "St Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20220622", "listing_expiration_date": "20261231"}