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"50580-726-32" National Drug Code (NDC)

Zyrtec Allergy 14 BLISTER PACK in 1 PACKAGE (50580-726-32) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)

NDC Code50580-726-32
Package Description14 BLISTER PACK in 1 PACKAGE (50580-726-32) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC50580-726
Product Type NameHUMAN OTC DRUG
Proprietary NameZyrtec Allergy
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20080101
Marketing Category NameNDA
Application NumberNDA019835
ManufacturerJohnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50580-726-32





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