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"50580-726-13" National Drug Code (NDC)
Zyrtec Allergy 3 BLISTER PACK in 1 CARTON (50580-726-13) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)
NDC Code
50580-726-13
Package Description
3 BLISTER PACK in 1 CARTON (50580-726-13) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
50580-726
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Zyrtec Allergy
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20080101
Marketing Category Name
NDA
Application Number
NDA019835
Manufacturer
Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50580-726-13