"71205-207-30" National Drug Code (NDC)

Cetirizine Hydrochloride 30 TABLET in 1 BOTTLE (71205-207-30)
(Proficient Rx LP)

NDC Code71205-207-30
Package Description30 TABLET in 1 BOTTLE (71205-207-30)
Product NDC71205-207
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20071227
Marketing Category NameANDA
Application NumberANDA078336
ManufacturerProficient Rx LP
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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