Package 24979-001-06

Brand: dexlansoprazole delayed release

Generic: dexlansoprazole
NDC Package

Package Facts

Identity

Package NDC 24979-001-06
Digits Only 2497900106
Product NDC 24979-001
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24979-001-06)

Marketing

Marketing Status
Marketed Since 2022-12-01
Brand dexlansoprazole delayed release
Generic dexlansoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "edb690de-04e9-4578-8af9-3ea6b0084489", "openfda": {"nui": ["N0000175525", "N0000000147"], "upc": ["0324979002064", "0324979001067"], "unii": ["UYE4T5I70X"], "rxcui": ["833204", "833213"], "spl_set_id": ["8dca4887-c75a-4021-8564-b704e9e1fa3e"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24979-001-06)", "package_ndc": "24979-001-06", "marketing_start_date": "20221201"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24979-001-07)", "package_ndc": "24979-001-07", "marketing_start_date": "20221201"}], "brand_name": "Dexlansoprazole delayed release", "product_id": "24979-001_edb690de-04e9-4578-8af9-3ea6b0084489", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "24979-001", "generic_name": "dexlansoprazole", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexlansoprazole", "brand_name_suffix": "delayed release", "active_ingredients": [{"name": "DEXLANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA202666", "marketing_category": "ANDA", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}