Package 68071-3776-6
Brand: pantoprazole
Generic: pantoprazolePackage Facts
Identity
Package NDC
68071-3776-6
Digits Only
6807137766
Product NDC
68071-3776
Description
60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3776-6)
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": "2cdd5c73-14c7-6010-e063-6394a90a83a1", "openfda": {"upc": ["0368071377668"], "unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["2bed1bae-519f-1bb9-e063-6294a90a795b"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3776-3)", "package_ndc": "68071-3776-3", "marketing_start_date": "20250129"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3776-6)", "package_ndc": "68071-3776-6", "marketing_start_date": "20250117"}], "brand_name": "Pantoprazole", "product_id": "68071-3776_2cdd5c73-14c7-6010-e063-6394a90a83a1", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-3776", "generic_name": "Pantoprazole", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077619", "marketing_category": "ANDA", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}