Package 68788-8536-3
Brand: rabeprazole sodium
Generic: rabeprazole sodiumPackage Facts
Identity
Package NDC
68788-8536-3
Digits Only
6878885363
Product NDC
68788-8536
Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8536-3)
Marketing
Marketing Status
Brand
rabeprazole sodium
Generic
rabeprazole sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7cadd193-627f-46b5-84f0-6d612b572ce5", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["4582d443-f1be-4f94-85da-49aa603f54e4"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8536-3)", "package_ndc": "68788-8536-3", "marketing_start_date": "20231019"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8536-6)", "package_ndc": "68788-8536-6", "marketing_start_date": "20231019"}], "brand_name": "RABEPRAZOLE SODIUM", "product_id": "68788-8536_7cadd193-627f-46b5-84f0-6d612b572ce5", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68788-8536", "generic_name": "rabeprazole sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RABEPRAZOLE SODIUM", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA204237", "marketing_category": "ANDA", "marketing_start_date": "20231019", "listing_expiration_date": "20261231"}