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"50580-728-52" National Drug Code (NDC)
Zyrtec-d 24 BLISTER PACK in 1 CARTON (50580-728-52) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(McNeil Consumer Healthcare Div McNeil-PPC, Inc)
NDC Code
50580-728-52
Package Description
24 BLISTER PACK in 1 CARTON (50580-728-52) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC
50580-728
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Zyrtec-d
Proprietary Name Suffix
Allergy And Congestion
Non-Proprietary Name
Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20080101
Marketing Category Name
NDA
Application Number
NDA021150
Manufacturer
McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name
CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength
5; 120
Strength Unit
mg/1; mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50580-728-52