Package 31722-032-32
Brand: pantoprazole sodium
Generic: pantoprazole sodiumPackage Facts
Identity
Package NDC
31722-032-32
Digits Only
3172203232
Product NDC
31722-032
Description
30 PACKET in 1 CARTON (31722-032-32) / 1 GRANULE, DELAYED RELEASE in 1 PACKET
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": "092a2d03-1a01-a7ac-e063-6394a90a01b4", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["ee6278c0-d8c0-417c-a65c-b522ff76fe44"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (31722-032-32) / 1 GRANULE, DELAYED RELEASE in 1 PACKET", "package_ndc": "31722-032-32", "marketing_start_date": "20231027"}], "brand_name": "Pantoprazole Sodium", "product_id": "31722-032_092a2d03-1a01-a7ac-e063-6394a90a01b4", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "31722-032", "generic_name": "Pantoprazole Sodium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA216139", "marketing_category": "ANDA", "marketing_start_date": "20231027", "listing_expiration_date": "20261231"}