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NDC 43063-0479-30 Levocetirizine Dihydrochloride 5 mg/1 Details

Levocetirizine Dihydrochloride 5 mg/1

Levocetirizine Dihydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is LEVOCETIRIZINE DIHYDROCHLORIDE.

MedlinePlus Drug Summary

Levocetirizine is used to relieve runny nose; sneezing; and redness, itching, and tearing of the eyes caused by hay fever, seasonal allergies, and allergies to other substances such as dust mites, animal dander, and mold. It is also used to treat symptoms of hives, including itching and rash. Levocetirizine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.

Related Packages: 43063-0479-30
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Levocetirizine

Product Information

NDC	43063-0479
Product ID	43063-479_0645be57-dd11-102b-e063-6294a90adc16
Associated GPIs	41550027100320
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	Levocetirizine Dihydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Levocetirizine Dihydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	LEVOCETIRIZINE DIHYDROCHLORIDE
Labeler Name	PD-Rx Pharmaceuticals, Inc.
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA090199
Listing Certified Through	2024-12-31

Package

NDC 43063-0479-30 (43063047930)

Pricing Information	N/A
NDC Package Code	43063-479-30
Billing NDC	43063047930
Package	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-479-30)
Marketing Start Date	2013-10-30
NDC Exclude Flag	N