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NDC 62250-0619-01 Desloratadine 5 mg/1 Details

Desloratadine 5 mg/1

Desloratadine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Belcher Pharmaceuticals,LLC. The primary component is DESLORATADINE.

MedlinePlus Drug Summary

Desloratadine is used in adults and children to relieve hay fever and allergy symptoms, including sneezing; runny nose; and red, itchy, tearing eyes. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash. Desloratadine is in a class of medications called antihistamines. It works by blocking histamine, a substance in the body that causes allergic symptoms.

Related Packages: 62250-0619-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Desloratadine

Product Information

NDC	62250-0619
Product ID	62250-619_06f9710a-798f-a99b-e063-6394a90a2e4b
Associated GPIs	41550021000320
GCN Sequence Number	047763
GCN Sequence Number Description	desloratadine TABLET 5 MG ORAL
HIC3	Z2Q
HIC3 Description	ANTIHISTAMINES - 2ND GENERATION
GCN	12762
HICL Sequence Number	021934
HICL Sequence Number Description	DESLORATADINE
Brand/Generic	Generic
Proprietary Name	Desloratadine
Proprietary Name Suffix	n/a
Non-Proprietary Name	Desloratadine
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	DESLORATADINE
Labeler Name	Belcher Pharmaceuticals,LLC
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078355
Listing Certified Through	2024-12-31

Package

NDC 62250-0619-01 (62250061901)

Pricing Information	N/A
NDC Package Code	62250-619-01
Billing NDC	62250061901
Package	30 TABLET in 1 BOTTLE (62250-619-01)
Marketing Start Date	2012-12-28
NDC Exclude Flag	N