Package 76420-668-30
Brand: pantoprazole sodium
Generic: pantoprazolePackage Facts
Identity
Package NDC
76420-668-30
Digits Only
7642066830
Product NDC
76420-668
Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-30)
Marketing
Marketing Status
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": "11517d51-eb1b-3d84-e063-6394a90a0bcd", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["ff15c4f1-8869-4422-9631-dc488e09e583"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-10)", "package_ndc": "76420-668-10", "marketing_start_date": "20240214"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-30)", "package_ndc": "76420-668-30", "marketing_start_date": "20240214"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-60)", "package_ndc": "76420-668-60", "marketing_start_date": "20240214"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-90)", "package_ndc": "76420-668-90", "marketing_start_date": "20240214"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "76420-668_11517d51-eb1b-3d84-e063-6394a90a0bcd", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "76420-668", "generic_name": "PANTOPRAZOLE", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20220501", "listing_expiration_date": "20261231"}