dexlansoprazole delayed release

Generic: dexlansoprazole

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexlansoprazole delayed release
Generic Name dexlansoprazole
Labeler bryant ranch prepack
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

dexlansoprazole 60 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2239
Product ID 72162-2239_e2456b53-466f-4dbc-bd4a-e21d5e487303
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202666
Listing Expiration 2026-12-31
Marketing Start 2022-12-01

Pharmacologic Class

Established (EPC)
proton pump inhibitor [epc]
Mechanism of Action
proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622239
Hyphenated Format 72162-2239

Supplemental Identifiers

RxCUI
833213
UNII
UYE4T5I70X
NUI
N0000175525 N0000000147

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dexlansoprazole delayed release (source: ndc)
Generic Name dexlansoprazole (source: ndc)
Application Number ANDA202666 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2239-3)
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2239-9)
source: ndc

Packages (2)

Ingredients (1)

dexlansoprazole (60 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e2456b53-466f-4dbc-bd4a-e21d5e487303", "openfda": {"nui": ["N0000175525", "N0000000147"], "unii": ["UYE4T5I70X"], "rxcui": ["833213"], "spl_set_id": ["dcfe880a-b96d-4a3c-aa21-3998d0bcfe9e"], "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 (72162-2239-3)", "package_ndc": "72162-2239-3", "marketing_start_date": "20221201"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2239-9)", "package_ndc": "72162-2239-9", "marketing_start_date": "20221201"}], "brand_name": "Dexlansoprazole delayed release", "product_id": "72162-2239_e2456b53-466f-4dbc-bd4a-e21d5e487303", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72162-2239", "generic_name": "dexlansoprazole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexlansoprazole", "brand_name_suffix": "delayed release", "active_ingredients": [{"name": "DEXLANSOPRAZOLE", "strength": "60 mg/1"}], "application_number": "ANDA202666", "marketing_category": "ANDA", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}