Package 72162-2244-3

Brand: dexlansoprazole

Generic: dexlansoprazole
NDC Package

Package Facts

Identity

Package NDC 72162-2244-3
Digits Only 7216222443
Product NDC 72162-2244
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2244-3)

Marketing

Marketing Status
Marketed Since 2024-01-29
Brand dexlansoprazole
Generic dexlansoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5a71d4c-fa7f-4689-acef-1462333db6db", "openfda": {"nui": ["N0000175525", "N0000000147"], "unii": ["UYE4T5I70X"], "rxcui": ["833204"], "spl_set_id": ["caad4ada-2cf9-4e12-99df-6ca4388cf0f6"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2244-3)", "package_ndc": "72162-2244-3", "marketing_start_date": "20240129"}], "brand_name": "Dexlansoprazole", "product_id": "72162-2244_b5a71d4c-fa7f-4689-acef-1462333db6db", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72162-2244", "generic_name": "Dexlansoprazole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexlansoprazole", "active_ingredients": [{"name": "DEXLANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA202294", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}