Package 72162-2214-3
Brand: dexlansoprazole
Generic: dexlansoprazolePackage Facts
Identity
Package NDC
72162-2214-3
Digits Only
7216222143
Product NDC
72162-2214
Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2214-3)
Marketing
Marketing Status
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": "f2ffd057-f79c-4337-9647-a9779b305b79", "openfda": {"nui": ["N0000175525", "N0000000147"], "unii": ["UYE4T5I70X"], "rxcui": ["833213"], "spl_set_id": ["3ed69e5a-aa78-4118-aa32-59a10f80c901"], "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 (72162-2214-3)", "package_ndc": "72162-2214-3", "marketing_start_date": "20240105"}], "brand_name": "Dexlansoprazole", "product_id": "72162-2214_f2ffd057-f79c-4337-9647-a9779b305b79", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72162-2214", "generic_name": "Dexlansoprazole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexlansoprazole", "active_ingredients": [{"name": "DEXLANSOPRAZOLE", "strength": "60 mg/1"}], "application_number": "ANDA202294", "marketing_category": "ANDA", "marketing_start_date": "20221122", "listing_expiration_date": "20261231"}