levocetirizine dihydrochloride

Product NDC
45802-594
11-digit product format
458020594
Labeler code
45802
Product ID
45802-594_5c926a5b-e80b-4e2c-bc1a-3af0451df199
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
levocetirizine dihydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Perrigo New York Inc
Application
ANDA090229
Marketing category
ANDA
Marketing start
2010-11-26
Marketing end
0000-00-00
Substance
LEVOCETIRIZINE DIHYDROCHLORIDE
Active strength
5 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
45802-594-01EA - Each45802-5947447ca93-0f96-4048-8404-c9b3df21dad312012-07-24
45802-594-65EA - Each45802-594ec740bc7-9ae6-4f0e-a305-1467bb17492f12012-07-24
45802-594-75EA - Each45802-59434f61e79-0336-48bb-ac96-8447e3a3ee1712012-07-24
45802-594-87EA - Each45802-5949b354b7e-cdb9-43b6-8245-d3f653a2532812012-07-24

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
45802-594-654580205946530 TABLET in 1 BOTTLE (45802-594-65) 30 tablet2010-11-260000-00-00NoNoCurrent