Package 31722-204-32
Brand: pantoprazole sodium
Generic: pantoprazole sodiumPackage Facts
Identity
Package NDC
31722-204-32
Digits Only
3172220432
Product NDC
31722-204
Description
25 VIAL, SINGLE-DOSE in 1 CARTON (31722-204-32) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (31722-204-31)
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": ["INTRAVENOUS"], "spl_id": "358ef102-b287-cdc7-e063-6394a90aa4a6", "openfda": {"upc": ["0331722204316"], "unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["1bb94d3c-8bc3-4193-9dd8-e9a22066707c"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (31722-204-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (31722-204-31)", "package_ndc": "31722-204-10", "marketing_start_date": "20220518"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (31722-204-32) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (31722-204-31)", "package_ndc": "31722-204-32", "marketing_start_date": "20220518"}], "brand_name": "pantoprazole sodium", "product_id": "31722-204_358ef102-b287-cdc7-e063-6394a90aa4a6", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "31722-204", "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": "ANDA213778", "marketing_category": "ANDA", "marketing_start_date": "20220518", "listing_expiration_date": "20261231"}