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"71205-709-20" National Drug Code (NDC)

Cetirizine Hydrochloride 20 TABLET, FILM COATED in 1 BOTTLE (71205-709-20)
(Proficient Rx LP)

NDC Code71205-709-20
Package Description20 TABLET, FILM COATED in 1 BOTTLE (71205-709-20)
Product NDC71205-709
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride Tablets
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181217
Marketing Category NameANDA
Application NumberANDA078343
ManufacturerProficient Rx LP
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/71205-709-20





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