"80539-002-09" National Drug Code (NDC)

Cetirizine Hydrochloride (allergy) 1 BOTTLE in 1 CARTON (80539-002-09) > 30 TABLET in 1 BOTTLE
(Allwell Health Inc)

NDC Code80539-002-09
Package Description1 BOTTLE in 1 CARTON (80539-002-09) > 30 TABLET in 1 BOTTLE
Product NDC80539-002
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride (allergy)
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20210215
Marketing Category NameANDA
Application NumberANDA090760
ManufacturerAllwell Health Inc
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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