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NDC 70934-0835-30 levocetirizine dihydrochloride 5 mg/1 Details

levocetirizine dihydrochloride 5 mg/1

levocetirizine dihydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. 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: 70934-0835-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Levocetirizine

Product Information

NDC	70934-0835
Product ID	70934-835_f1d83733-9b02-0d6b-e053-2a95a90abe84
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	levocetirizine dihydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	levocetirizine dihydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	LEVOCETIRIZINE DIHYDROCHLORIDE
Labeler Name	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA203646
Listing Certified Through	n/a

Package

NDC 70934-0835-30 (70934083530)

Pricing Information	N/A
NDC Package Code	70934-835-30
Billing NDC	70934083530
Package	30 TABLET in 1 BOTTLE, PLASTIC (70934-835-30)
Marketing Start Date	2021-03-05
NDC Exclude Flag	N