Package 31722-713-10
Brand: pantoprazole sodium
Generic: pantoprazolePackage Facts
Identity
Package NDC
31722-713-10
Digits Only
3172271310
Product NDC
31722-713
Description
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-10)
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": "48f42a12-2eac-e5dd-e063-6294a90aa92d", "openfda": {"upc": ["0331722713900", "0331722712903"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["9daa1483-5a36-44db-9e0d-904d100da262"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-10)", "package_ndc": "31722-713-10", "marketing_start_date": "20140910"}, {"sample": false, "description": "10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-713-31)", "package_ndc": "31722-713-31", "marketing_start_date": "20140910"}, {"sample": false, "description": "10 TABLET, DELAYED RELEASE in 1 CARTON (31722-713-32)", "package_ndc": "31722-713-32", "marketing_start_date": "20140910"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-90)", "package_ndc": "31722-713-90", "marketing_start_date": "20140910"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "31722-713_48f42a12-2eac-e5dd-e063-6294a90aa92d", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "31722-713", "generic_name": "PANTOPRAZOLE", "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": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20271231"}