Package 72603-317-30
Brand: pantoprazole sodium
Generic: pantoprazole sodiumPackage Facts
Identity
Package NDC
72603-317-30
Digits Only
7260331730
Product NDC
72603-317
Description
30 PACKET in 1 CARTON (72603-317-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (72603-317-01)
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": "4494f9d0-a1c8-477f-9b4a-f65d7637d9ec", "openfda": {"upc": ["0372603317015"], "unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["4494f9d0-a1c8-477f-9b4a-f65d7637d9ec"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (72603-317-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (72603-317-01)", "package_ndc": "72603-317-30", "marketing_start_date": "20241001"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "72603-317_4494f9d0-a1c8-477f-9b4a-f65d7637d9ec", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72603-317", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA213725", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}