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NDC 50090-4794-01 DESLORATADINE 5 mg/1 Details

DESLORATADINE 5 mg/1

DESLORATADINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. 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: 50090-4794-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Desloratadine

Product Information

NDC	50090-4794
Product ID	50090-4794_a9437daf-a970-4965-9f90-1c9c85ca030b
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	DESLORATADINE
Proprietary Name Suffix	n/a
Non-Proprietary Name	DESLORATADINE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	DESLORATADINE
Labeler Name	A-S Medication Solutions
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078352
Listing Certified Through	2024-12-31

Package

NDC 50090-4794-01 (50090479401)

Pricing Information	N/A
NDC Package Code	50090-4794-1
Billing NDC	50090479401
Package	30 TABLET, FILM COATED in 1 BOTTLE (50090-4794-1)
Marketing Start Date	2019-12-12
NDC Exclude Flag	N