NDC 72162-2308-01 - Desloratadine

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
72162-2308
Requested NDC
72162-2308-01
Package NDCs from labels
72162-2308-1, 72162-2308-3, 72162-2308-5, 72162-2308-01
Manufacturer
Bryant Ranch Prepack
Effective date
2025-11-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Desloratadine - Bryant Ranch PrepackBryant Ranch Prepack2025-11-06HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-2308-1Desloratadine100 in 1 BOTTLE, PLASTICTABLET100102
72162-2308-3Desloratadine30 in 1 BOTTLE, PLASTICTABLET30102
72162-2308-5Desloratadine500 in 1 BOTTLE, PLASTICTABLET500102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-2308DESLORATADINE TABLET [BRYANT RANCH PREPACK]101Current NDC, 3 package rows20240606_cf7f838b-4595-4c81-97b9-e1594347e1bd.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-2308-1EA - Each72162-23084ba93093-d5fb-4cda-9c84-b9852fa7117a12024-06-10
72162-2308-3EA - Each72162-2308ab83f108-f697-4abb-a82b-5f3ef36cc11d12024-10-04
72162-2308-5EA - Each72162-2308f2088eab-6153-4d2c-9a7c-40acc4eca90c12024-06-10

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 2 · 22 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DesloratadineDESLORATADINEA-S Medication Solutions36307c2b-6b6a-46a9-9fe4-1798fc72e7b82023-12-12Warnings, Adverse reactionsExact identifier
application number: ANDA078355
rxcui: 349420
unii: FVF865388R
DesloratadineDESLORATADINEBionpharma Inc.4d094001-b85a-47b3-bc67-a46660384ece2023-11-27Warnings, Adverse reactionsExact identifier
rxcui: 349420
unii: FVF865388R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.